Name

RNU7-36P Gene

RNA, U7 small nuclear 36 pseudogene

CTD-3080P12.3 Gene

uncharacterized LOC101928857

RNU6-36P Gene

RNA, U6 small nuclear 36, pseudogene

CH17-340M24.3 Gene

uncharacterized protein BC009467

RNU7-32P Gene

RNA, U7 small nuclear 32 pseudogene

RNU7-33P Gene

RNA, U7 small nuclear 33 pseudogene

RNU6-39P Gene

RNA, U6 small nuclear 39, pseudogene

RNU7-38P Gene

RNA, U7 small nuclear 38 pseudogene

RNU7-30P Gene

RNA, U7 small nuclear 30 pseudogene

RNU6-31P Gene

RNA, U6 small nuclear 31, pseudogene

RNU7-35P Gene

RNA, U7 small nuclear 35 pseudogene

RNU6-34P Gene

RNA, U6 small nuclear 34, pseudogene

CH17-351M24.1 Gene

uncharacterized LOC644767

DUPXQ27.3Q28 Gene

Chromosome Xq27.3-q28 duplication syndrome

RNU7-37P Gene

RNA, U7 small nuclear 37 pseudogene

CTB-30L5.1 Gene

uncharacterized LOC102724339

RNU6-35P Gene

RNA, U6 small nuclear 35, pseudogene

CH17-360D5.1 Gene

neuropeptide Y receptor type 4-like

RNU7-34P Gene

RNA, U7 small nuclear 34 pseudogene

CTC-338M12.4 Gene

uncharacterized LOC101928649

RNU6-30P Gene

RNA, U6 small nuclear 30, pseudogene

CTB-3M24.3 Gene

uncharacterized LOC105379180

RNU7-39P Gene

RNA, U7 small nuclear 39 pseudogene

RNU7-31P Gene

RNA, U7 small nuclear 31 pseudogene

MIR7-3HG Gene

MIR7-3 host gene

RNU6-33P Gene

RNA, U6 small nuclear 33, pseudogene

MGR3 Gene

Migraine, familial, with or without aura, susceptibility to

MGR5 Gene

Migraine with or without aura, susceptibility to, 5

MGR12 Gene

Migraine, with or without aura, susceptibility to, 12

MGR7 Gene

Migraine with aura, susceptibility to, 7

MGR9 Gene

Migraine with aura, susceptibility to, 9

MGR1 Gene

Migraine with aura, susceptibility to

ETL4 Gene

epilepsy, occipitotemporal lobe, and migraine with aura

MGR2 Gene

Migraine, familial typical, susceptibility to

MGR8 Gene

Migraine, susceptibility to, 8

MGR4 Gene

Migraine, susceptibility to, 4

OS4 Gene

Osteoarthritis, generalized, without dysplasia, susceptibility to

CTEPH1 Gene

Pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to

MGR6 Gene

Migraine, several forms

TNFRSF10C Gene

tumor necrosis factor receptor superfamily, member 10c, decoy without an intracellular domain

The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contains an extracellular TRAIL-binding domain and a transmembrane domain, but no cytoplasmic death domain. This receptor is not capable of inducing apoptosis, and is thought to function as an antagonistic receptor that protects cells from TRAIL-induced apoptosis. This gene was found to be a p53-regulated DNA damage-inducible gene. The expression of this gene was detected in many normal tissues but not in most cancer cell lines, which may explain the specific sensitivity of cancer cells to the apoptosis-inducing activity of TRAIL. [provided by RefSeq, Jul 2008]

LILRA3 Gene

leukocyte immunoglobulin-like receptor, subfamily A (without TM domain), member 3

This gene encodes a member of a family of immunoreceptors that are expressed predominantly in monocytes and B cells, and at lower levels in dendritic cells and natural killer cells. The encoded protein lacks the transmembrane region found in other members of this family. It acts as a soluble receptor for class I major histocompatibility complex (MHC) antigens. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and is polymorphic in human populations, with many individuals containing a deletion of this genomic region. [provided by RefSeq, Mar 2014]

RIT2 Gene

Ras-like without CAAX 2

RIN belongs to the RAS (HRAS; MIM 190020) superfamily of small GTPases (Shao et al., 1999 [PubMed 10545207]).[supplied by OMIM, Mar 2008]

RIT1 Gene

Ras-like without CAAX 1

This gene encodes a member of a subfamily of Ras-related GTPases. The encoded protein is involved in regulating p38 MAPK-dependent signaling cascades related to cellular stress. This protein also cooperates with nerve growth factor to promote neuronal development and regeneration. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]

HTGH Gene

Hypertrichosis terminalis, generalized, with or without gingival hyperplasia

RPH3AL Gene

rabphilin 3A-like (without C2 domains)

The protein encoded by this gene plays a direct regulatory role in calcium-ion-dependent exocytosis in both endocrine and exocrine cells and plays a key role in insulin secretion by pancreatic cells. This gene is likely a tumor suppressor. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jun 2010]

ANOP1 Gene

anophthalmos 1 (with mental retardation, without limb anomalies or dental or urogenital abnormalities)

BMIQ7 Gene

Obesity, susceptibility to, on chromosome 4

ASPG2 Gene

Asperger syndrome, susceptibility to, 2

ASPG3 Gene

Asperger syndrome, susceptibility to, 3

ASPG4 Gene

Asperger syndrome, susceptibility to, 4

ATOD7 Gene

Dermatitis, atopic, susceptibility to, 7

ENDO1 Gene

Endometriosis, susceptibility to, 1

HYT3 Gene

Hypertension, essential, susceptibility to, 3

HYT5 Gene

Hypertension, essential, susceptibility to, 5

HYT4 Gene

Hypertension, essential, susceptibility to, 4

HYT7 Gene

Hypertension, essential, susceptibility to, 7

HYT6 Gene

Hypertension, essential, susceptibility to, 6

HYT8 Gene

hypertension, essential, susceptibility to, 8

GRD2 Gene

Graves disease, susceptibility to, 2

GRDX Gene

Graves disease, susceptibility to, X-linked

EIG4 Gene

Epilepsy, idiopathic generalized, susceptibility to 4

PRAC2 Gene

prostate cancer susceptibility candidate 2

This gene is highly expressed in prostate, rectum, colon, and testis. This gene may produce a non-coding RNA or may encode a short protein that might localize to the nucleus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

PRAC1 Gene

prostate cancer susceptibility candidate 1

This gene is reported to be specifically expressed in prostate, rectum and distal colon. Sequence analysis suggests that it may play a regulatory role in the nucleus. [provided by RefSeq, Jul 2008]

SS3 Gene

Sarcoidosis, susceptibility to, 3

BMIQ10 Gene

Obesity, susceptibility to, on chromosome 10q

PSORS9 Gene

psoriasis susceptibility 9

PSORS8 Gene

psoriasis susceptibility 8

PSORS7 Gene

psoriasis susceptibility 7

PSORS6 Gene

psoriasis susceptibility 6

PSORS5 Gene

psoriasis susceptibility 5

PSORS4 Gene

psoriasis susceptibility 4

PSORS3 Gene

psoriasis susceptibility 3

NKS1 Gene

natural killer cell susceptibility 1

CELIAC8 Gene

Celiac disease, susceptibility to, 8

CELIAC5 Gene

Celiac disease, susceptibility to, 5

CELIAC6 Gene

Celiac disease, susceptibility to, 6

CELIAC7 Gene

Celiac disease, susceptibility to, 7

AIS3 Gene

autoimmune susceptibility 3 (vitiligo specific)

AIS2 Gene

autoimmune susceptibility 2

AIS1 Gene

autoimmune susceptibility 1

AIS4 Gene

autoimmune disease, susceptibility to, 4

SLEB13 Gene

Systemic lupus erythematosus, susceptibility to, 13

SLEB12 Gene

Systemic lupus erythematosus, susceptibility to, 12

SLEB15 Gene

Systemic lupus erthematosus, susceptibility to, 15

CIHL Gene

hearing loss, cisplatin-induced, susceptibility to

IGAD1 Gene

immunoglobulin A (IgA) deficiency susceptibility 1

OS6 Gene

Osteoarthritis susceptibility 6

CASC4P1 Gene

cancer susceptibility candidate 4 pseudogene 1

BCC5 Gene

Basal cell carcinoma, susceptibility to, 5

NBLST5 Gene

Neuroblastoma, susceptibility to, 5

NBLST4 Gene

Neuroblastoma, susceptibility to, 4

NBLST6 Gene

Neuroblastoma, susceptibility to, 6

MAFD9 Gene

Major affective disorder-9, susceptibility to

MAFD8 Gene

Major affective disorder-8, susceptibility to

IGAN2 Gene

IgA nephropathy, susceptibility to, 2

AUTS6 Gene

Autism, susceptibility to, 6

AUTS7 Gene

Autism, susceptibility to, 7

AUTS5 Gene

Autism, susceptibility to, 5

AUTS2 Gene

autism susceptibility candidate 2

This gene has been implicated in neurodevelopment and as a candidate gene for numerous neurological disorders, including autism spectrum disorders, intellectual disability, and developmental delay. Mutations in this gene have also been associated with non-neurological disorders, such as acute lymphoblastic leukemia, aging of the skin, early-onset androgenetic alopecia, and certain cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2014]

AUTS3 Gene

Autism, susceptibility to, 3

AUTS1 Gene

Autism, susceptibility to, 1

AUTS8 Gene

Autism, susceptibility to, 8

EIG3 Gene

Epilepsy, idiopathic generalized, susceptibility to 3

EIG2 Gene

Epilepsy, idiopathic generalized, susceptibility to 2

CASC2 Gene

cancer susceptibility candidate 2 (non-protein coding)

CASC1 Gene

cancer susceptibility candidate 1

CASC6 Gene

cancer susceptibility candidate 6 (non-protein coding)

CASC5 Gene

cancer susceptibility candidate 5

The protein encoded by this gene is a component of the multiprotein assembly that is required for creation of kinetochore-microtubule attachments and chromosome segregation. The encoded protein functions as a scaffold for proteins that influence the spindle assembly checkpoint during the eukaryotic cell cycle and it interacts with at least five different kinetochore proteins and two checkpoint kinases. In adults, this gene is predominantly expressed in normal testes, various cancer cell lines and primary tumors from other tissues and is ubiquitously expressed in fetal tissues. This gene was originally identified as a fusion partner with the mixed-lineage leukemia (MLL) gene in t(11;15)(q23;q14). Mutations in this gene cause autosomal recessive primary microcephaly-4 (MCPH4). Alternative splicing results in multiple transcript variants encoding different isoforms. Additional splice variants have been described but their biological validity has not been confirmed. [provided by RefSeq, Jan 2013]

CASC4 Gene

cancer susceptibility candidate 4

The increased expression level of this gene is associated with HER-2/neu proto-oncogene overexpression. Amplification and resulting overexpression of this proto-oncogene are found in approximately 30% of human breast and 20% of human ovarian cancers. Alternatively spliced variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Dec 2010]

CASC8 Gene

cancer susceptibility candidate 8 (non-protein coding)

HYT1 Gene

Hypertension, essential, susceptibility to, 1

HYT2 Gene

Hypertension, essential, susceptibility to, 2

BCC6 Gene

Basal cell carcinoma, susceptibility to, 6

CASC18 Gene

cancer susceptibility candidate 18 (non-protein coding)

ADHD2 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 2

CLLS1 Gene

Leukemia, chronic lymphocytic, susceptibility to, 1

LOC101930332 Gene

autism susceptibility gene 2 protein-like

ASRT8 Gene

Asthma-related traits, susceptibility to, 8

OVCAS1 Gene

Ovarian cancer, epithelial, susceptibility to

OMS Gene

otitis media, susceptibility to

EIG5 Gene

Epilepsy, idiopathic generalized, susceptibility to, 5

KAZA1 Gene

Kala-azar (visceral leishmaniasis), susceptibility to

KAZA2 Gene

Kala-azar, susceptibility to, 2

KAZA3 Gene

Kala-azar, susceptibility to, 3

DYX5 Gene

dyslexia susceptibility 5

PSORS1C1 Gene

psoriasis susceptibility 1 candidate 1

This gene is one of several genes thought to confer susceptibility to psoriasis and systemic sclerosis, located on chromosome 6 near the major histocompatibility complex (MHC) class I region. [provided by RefSeq, Sep 2011]

PSORS1C3 Gene

psoriasis susceptibility 1 candidate 3 (non-protein coding)

PSORS1C2 Gene

psoriasis susceptibility 1 candidate 2

AUTS11 Gene

Autism, susceptibility to, 11

AUTS12 Gene

autism, susceptibility to, 12

AUTS13 Gene

autism, susceptibility to, 13

HPC6 Gene

Prostate cancer, susceptibility to

MTBS3 Gene

Mycobacterium tuberculosis, susceptibility to, 3

MTBS2 Gene

Mycobacterium tuberculosis, susceptibility to, 2

MTBS1 Gene

mycobacterium tuberculosis, susceptibility to infection by, 1

MTBSX Gene

Mycobacterium tuberculosis, susceptibility to infection by

CASC3 Gene

cancer susceptibility candidate 3

The product of this gene is a core component of the exon junction complex (EJC), a protein complex that is deposited on spliced mRNAs at exon-exon junctions and functions in nonsense-mediated mRNA decay (NMD). The encoded protein binds RNA and interacts with two other EJC core components. It is predominantly located in the cytoplasm, but shuttles into the nucleus where it localizes to nuclear speckles. [provided by RefSeq, Jul 2008]

CASC7 Gene

cancer susceptibility candidate 7 (non-protein coding)

CASC9 Gene

cancer susceptibility candidate 9 (non-protein coding)

CHDS4 Gene

Coronary heart disease, susceptibility to, 4

CLLS3 Gene

Leukemia, chronic lymphocytic, susceptibility to, 3

CASC11 Gene

cancer susceptibility candidate 11 (non-protein coding)

CASC10 Gene

cancer susceptibility candidate 10

CASC17 Gene

cancer susceptibility candidate 17 (non-protein coding)

CASC16 Gene

cancer susceptibility candidate 16 (non-protein coding)

CASC15 Gene

cancer susceptibility candidate 15 (non-protein coding)

CASC19 Gene

cancer susceptibility candidate 19 (non-protein coding)

ADHD4 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 4

ADHD5 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 5

ADHD6 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 6

ADHD1 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 1

ADHD3 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 2

ASOBS Gene

Asthma and obesity susceptibility, chromosome 16p11 inversion related

BULN Gene

Bulimia nervosa, susceptibility to

ALL2 Gene

Leukemia, acute lymphoblastic, susceptibility to, 2

GLM6 Gene

Glioma susceptibility 6

GLM7 Gene

Glioma susceptibility 7

GLM5 Gene

Glioma susceptibility 5

GLM8 Gene

Glioma susceptibility 8

STBMS1 Gene

Strabismus, susceptibility to, 1

IS5 Gene

scoliosis, idiopathic, susceptibility to, 5

IS4 Gene

Scoliosis, idiopathic, susceptibility to, 4

CRCS10 Gene

Colorectal cancer, susceptibility to, 10

CRCS11 Gene

Colorectal cancer, susceptibility to, 11

NPCA2 Gene

Nasopharyngeal carcinoma, susceptibility to, 2

SM2 Gene

Hepatic fibrosis susceptibility due to Schistosoma mansoni infection

SM1 Gene

Schistosoma mansoni, susceptibility/resistance to

PDCOS Gene

Podoconiosis, susceptibility to

DEL16P11.2 Gene

autism, susceptibility to, 14

BTS1 Gene

bladder tumor susceptibility 1

PTCSC1 Gene

papillary thyroid carcinoma susceptibility candidate 1 (non-protein coding)

PTCSC3 Gene

papillary thyroid carcinoma susceptibility candidate 3 (non-protein coding)

CASC23 Gene

cancer susceptibility candidate 23 (non-protein coding)

CASC22 Gene

cancer susceptibility candidate 22 (non-protein coding)

CASC20 Gene

cancer susceptibility candidate 20 (non-protein coding)

CASC21 Gene

cancer susceptibility candidate 21 (non-protein coding)

CRCS8 Gene

Colorectal cancer, susceptibility to, 8

CRCS9 Gene

colorectal cancer, susceptibility to, 9

CRCS2 Gene

Colorectal cancer, susceptibility to, 2

CRCS5 Gene

Colorectal cancer, susceptibility to, 5

MBNP Gene

?Membranous nephropathy, susceptibility to

NAFLD2 Gene

Fatty liver disease, nonalcoholic, susceptibility to, 2

ANON1 Gene

Anorexia nervosa, susceptibility to, 1

BCC4 Gene

Basal cell carcinoma, susceptibility to, 4

CMM7 Gene

Melanoma, cutaneous malignant, susceptibility to, 7

LNCR3 Gene

Lung cancer susceptibility 3

LNCR4 Gene

Lung cancer susceptibility 4

LNCR5 Gene

Lung cancer susceptibility 5

CLLS4 Gene

Leukemia, chronic lymphocytic susceptibility to, 4

AITD2 Gene

Autoimmune thyroid disease, susceptibility to, 2

AITD1 Gene

Autoimmune thyroid disease, susceptibility to, 1

AITD4 Gene

Autoimmune thyroid disease, susceptibility to, 4

ASRT6 Gene

Asthma-related traits, susceptibility to, 6

ASRT4 Gene

Asthma-related traits, susceptibility to, 4

MS3 Gene

Multiple sclerosis, susceptibility to, 3

MS2 Gene

Multiple sclerosis, susceptibility to, 2

DYX9 Gene

dyslexia susceptibility 9

DYX8 Gene

dyslexia susceptibility 8

MHS6 Gene

malignant hyperthermia susceptibility 6

MHS4 Gene

malignant hyperthermia susceptibility 4

MHS2 Gene

malignant hyperthermia susceptibility 2

MHS3 Gene

Malignant hyperthermia susceptibility 3

TSG101 Gene

tumor susceptibility 101

The protein encoded by this gene belongs to a group of apparently inactive homologs of ubiquitin-conjugating enzymes. The gene product contains a coiled-coil domain that interacts with stathmin, a cytosolic phosphoprotein implicated in tumorigenesis. The protein may play a role in cell growth and differentiation and act as a negative growth regulator. In vitro steady-state expression of this tumor susceptibility gene appears to be important for maintenance of genomic stability and cell cycle regulation. Mutations and alternative splicing in this gene occur in high frequency in breast cancer and suggest that defects occur during breast cancer tumorigenesis and/or progression. [provided by RefSeq, Jul 2008]

HDPA Gene

Hodgkin disease, susceptibility, pseudoautosomal

ASPG1 Gene

Asperger syndrome, susceptibility to, 1

SCZD14 Gene

schizophrenia, susceptibility to, 14

SCZD11 Gene

Schizophrenia susceptibility locus, chromosome 10q-related

LOC100288160 Gene

esophagus cancer-related gene-2 interaction susceptibility protein

BCC1 Gene

Basal cell carcinoma, susceptibility to, 1

BCC2 Gene

Basal cell carcinoma, susceptibility to, 2

BCC3 Gene

Basal cell carcinoma, susceptibility to, 3

ODS1 Gene

Opioid dependence, susceptibility to, 1

PARK16 Gene

Parkinson disease 16 (susceptibility)

PARK10 Gene

Parkinson disease 10 (susceptibility)

PARK12 Gene

Parkinson disease 12 (susceptibility)

PDA1 Gene

Patent ductus arteriosus, susceptibility to

LPRS Gene

Leprosy, susceptibility to 1

CRCS6 Gene

colorectal cancer, susceptibility to, 6

MMS Gene

Malignant mesothelioma, susceptibility to

DYX1C1 Gene

dyslexia susceptibility 1 candidate 1

This gene encodes a tetratricopeptide repeat domain-containing protein. The encoded protein interacts with estrogen receptors and the heat shock proteins, Hsp70 and Hsp90. An homologous protein in rat has been shown to function in neuronal migration in the developing neocortex. A chromosomal translocation involving this gene is associated with a susceptibility to developmental dyslexia. Mutations in this gene are associated with deficits in reading and spelling. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream cell cycle progression 1 (CCPG1) gene. [provided by RefSeq, Mar 2011]

HSCR9 Gene

Hirschsprung disease, susceptibility to, 9

HSCR5 Gene

Hirschsprung disease, susceptibility to, 5

The disorder described by Hirschsprung (1888) and known as Hirschsprung disease or aganglionic megacolon is characterized by congenital absence of intrinsic ganglion cells in the myenteric (Auerbach) and submucosal (Meissner) plexuses of the gastrointestinal tract. Patients are diagnosed with the short-segment form (S-HSCR, approximately 80% of cases) when the aganglionic segment does not extend beyond the upper sigmoid, and with the long-segment form (L-HSCR) when aganglionosis extends proximal to the sigmoid. Total colonic aganglionosis and total intestinal HSCR also occur (Amiel et al., 2008 [PubMed 17965226]). Isolated HSCR appears to be of complex nonmendelian inheritance with low sex-dependent penetrance and variable expression according to the length of the aganglionic segment, suggestive of the involvement of one or more genes with low penetrance (Amiel et al., 2008 [PubMed 17965226]). For a general description and a discussion of genetic heterogeneity of Hirschsprung disease (HSCR), see MIM 142623.[supplied by OMIM, Feb 2011]

PTCSC2 Gene

papillary thyroid carcinoma susceptibility candidate 2 (non-protein coding)

DYX1 Gene

dyslexia susceptibility 1

DYX3 Gene

dyslexia susceptibility 3

DYX4 Gene

dyslexia susceptibility 4

DYX7 Gene

dyslexia susceptibility 7

DYX6 Gene

dyslexia susceptibility 6

FL1 Gene

Follicular lymphoma, susceptibility to, 1

TGCT1 Gene

testicular germ cell tumor susceptibility 1

DELXP22.11 Gene

Autism, X-linked, susceptibility to, 4

ASRT3 Gene

Asthma-related traits, susceptibility to, 3

RLS1 Gene

Restless legs syndrome, susceptibility to

RLS6 Gene

Restless legs syndrome, susceptibility to, 6

RLS5 Gene

Restless legs syndrome, susceptibility to, 5

RLS8 Gene

Restless legs syndrome, susceptibility to, 8

CELIAC9 Gene

Celiac disease, susceptibility to, 9

ALL1 Gene

Leukemia, acute lymphocytic, susceptibility to, 1

LOAS Gene

Leber optic atrophy, susceptibility to

SLEB4 Gene

systemic lupus erythematosus, susceptibility to, 4

UVM2 Gene

Melanoma, uveal, susceptibility to, 2

UVM1 Gene

Melanoma, uveal, susceptibility to, 1

ARMS2 Gene

age-related maculopathy susceptibility 2

This gene encodes a protein that is thought to play a role in diseases in the elderly. Mutations in this gene have been associated with age-related macular degeneration. [provided by RefSeq, Oct 2008]

ATHS Gene

atherosclerosis susceptibility (lipoprotein associated)

WM2 Gene

Macroglobulinemia, Waldenstrom, susceptibility to, 2

CMTS Gene

Chronic mountain sickness, susceptibility to

CHDS3 Gene

Coronary heart disease, susceptibility to, 3

CHDS2 Gene

Coronary heart disease, susceptibility to, 2

CHDS1 Gene

Coronary heart disease, susceptibility to, 1

CHDS8 Gene

Coronary heart disease, susceptibility to, 8

HHV8S Gene

Human herpesvirus 8, susceptibility to

IDDMX Gene

Diabetes mellitus, insulin-dependent, X-linked, susceptibility to

SLEB5 Gene

Systemic lupus erythematosus, susceptibility to, 5

SLEB8 Gene

Systemic lupus erythematosus, susceptibility to, 8

PSORS11 Gene

Psoriasis susceptibility 11

PSORS10 Gene

psoriasis susceptibility 10

SPDA3 Gene

Spondylarthropathy, susceptibility to, 3

SPDA2 Gene

Spondyloarthropathy, susceptibility to, 2

WM1 Gene

Macroglobulinemia, Waldenstrom, susceptibility to, 1

CRCS7 Gene

colorectal cancer, susceptibility to, 7

CELIAC12 Gene

Celiac disease, susceptibility to, 12

CELIAC13 Gene

Celiac disease, susceptibility to, 13

CELIAC10 Gene

Celiac disease, susceptibility to, 10

CELIAC11 Gene

Celiac disease, susceptibility to, 11

PVOP1 Gene

Pelvic organ prolapse, susceptibility to, 1

PVOP2 Gene

Pelvic organ prolapse, susceptibility to, 2

SLEB3 Gene

systemic lupus erythematosus susceptibility 3

SLEB7 Gene

Systemic lupus erythematosus, susceptibility to, 7

{migraine with or without aura, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine with or without aura, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

migraine disorders; migraine with aura; migraine without aura; tension-type headache Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders; migraine with aura; migraine without aura; tension-type headache in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine disorders; migraine with aura; migraine without aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders; migraine with aura; migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine with aura; migraine without aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine with aura; migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

{migraine without aura, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine without aura, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine, with or without aura, susceptibility to, 12} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine, with or without aura, susceptibility to, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine without aura, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine without aura, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine with or without aura, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine with or without aura, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine with or without aura, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine with or without aura, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine, with or without aura, susceptibility to, 13} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine, with or without aura, susceptibility to, 13} phenotype from the curated OMIM Gene-Disease Associations dataset.

migraine with or without aura, susceptibility to Gene Set

From OMIM Gene-Disease Associations

genes associated with the migraine with or without aura, susceptibility to phenotype from the curated OMIM Gene-Disease Associations dataset.

migraine disorders; migraine with aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders; migraine with aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine; migraine with aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine; migraine with aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; migraine disorders; migraine with aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; migraine disorders; migraine with aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Migraine without Aura Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Migraine without Aura from the curated CTD Gene-Disease Associations dataset.

Migraine without Aura Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Migraine without Aura in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

migraine without aura Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease migraine without aura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

migraine without aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine with and without aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine with and without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Migraine without aura Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Migraine without aura phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

migraine without aura Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease migraine without aura in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

migraine without aura Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the migraine without aura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

migraine without aura Gene Set

From HPO Gene-Disease Associations

genes associated with the migraine without aura phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Migraine without Aura Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Migraine without Aura phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

{migraine with aura, susceptibility to, 9} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine with aura, susceptibility to, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine with aura, susceptibility to, 7} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine with aura, susceptibility to, 7} phenotype from the curated OMIM Gene-Disease Associations dataset.

Migraine with Aura Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Migraine with Aura from the curated CTD Gene-Disease Associations dataset.

migraine with aura Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease migraine with aura from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

migraine with aura Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease migraine with aura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

migraine with aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine with aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; embolism, paradoxical; heart septal defects, atrial; migraine with aura; stroke; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; embolism, paradoxical; heart septal defects, atrial; migraine with aura; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Migraine with aura Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Migraine with aura phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

migraine with aura Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease migraine with aura in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

migraine with aura Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the migraine with aura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

migraine with aura Gene Set

From HPO Gene-Disease Associations

genes associated with the migraine with aura phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Migraine with Aura Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Migraine with Aura phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

{migraine, susceptibility to, 8} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine, familial typical, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine, familial typical, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

{pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aura anxiety and depression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aura anxiety and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aura Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term aura in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

migraine disorders(c10.228.140.546.399.750)/genetics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders(c10.228.140.546.399.750)/genetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Familial hemiplegic migraine type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hemiplegic migraine type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hemiplegic migraine type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hemiplegic migraine type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hemiplegic migraine type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hemiplegic migraine type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Migraine, familial basilar Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Migraine, familial basilar phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Migraine, Familial Hemiplegic, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Migraine, Familial Hemiplegic, 3 from the curated CTD Gene-Disease Associations dataset.

Migraine Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Migraine Disorders from the curated CTD Gene-Disease Associations dataset.

MIGRAINE, FAMILIAL HEMIPLEGIC, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 2 from the curated CTD Gene-Disease Associations dataset.

MIGRAINE, FAMILIAL HEMIPLEGIC, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 1 from the curated CTD Gene-Disease Associations dataset.

Hemiplegic migraine, familial type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemiplegic migraine, familial type 2 from the curated CTD Gene-Disease Associations dataset.

Hemiplegic migraine, familial type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemiplegic migraine, familial type 1 from the curated CTD Gene-Disease Associations dataset.

Migraine Disorders Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Migraine Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

familial hemiplegic migraine Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease familial hemiplegic migraine from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

migraine Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease migraine from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

migraine Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease migraine in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

familial hemiplegic migraine Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease familial hemiplegic migraine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

migraine Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease migraine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

migraine disorders; tension-type headache Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders; tension-type headache in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy; migraine disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine disorders; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; migraine disorders; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; migraine disorders; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; intracranial thrombosis; ischemic attack, transient; migraine disorders; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; intracranial thrombosis; ischemic attack, transient; migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cadasil; cardiovascular diseases; hypertension; migraine disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cadasil; cardiovascular diseases; hypertension; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemiplegia; migraine disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemiplegia; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine, hemiplegic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine, hemiplegic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; cadasil; migraine disorders; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; cadasil; migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; migraine disorders; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; migraine disorders; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine disorders; syndrome; vomiting Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders; syndrome; vomiting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intracranial embolism; migraine disorders; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intracranial embolism; migraine disorders; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; migraine disorders; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial hemiplegic migraine and benign familial infantile convulsions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammation; migraine disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammation; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; migraine disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

panic disorder; migraine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease panic disorder; migraine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

headache; migraine disorders; neurogenic inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease headache; migraine disorders; neurogenic inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

metabolic diseases; migraine disorders; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease metabolic diseases; migraine disorders; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine disorders; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain injuries; cerebrovascular disorders; migraine disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain injuries; cerebrovascular disorders; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

typical migraine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease typical migraine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term migraine in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Migraine Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Migraine phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Migraine - clinic-based Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Migraine - clinic-based phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

migraine Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease migraine in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

migraine Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the migraine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

migraine Gene Set

From HPO Gene-Disease Associations

genes associated with the migraine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Migraine Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Migraine Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

migraine, familial basilar Gene Set

From OMIM Gene-Disease Associations

genes associated with the migraine, familial basilar phenotype from the curated OMIM Gene-Disease Associations dataset.

migraine, resistance to Gene Set

From OMIM Gene-Disease Associations

genes associated with the migraine, resistance to phenotype from the curated OMIM Gene-Disease Associations dataset.

migraine, familial hemiplegic, 1, with progressive cerebellar ataxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the migraine, familial hemiplegic, 1, with progressive cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.

migraine, familial hemiplegic, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the migraine, familial hemiplegic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

migraine, familial hemiplegic, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the migraine, familial hemiplegic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

migraine, familial hemiplegic, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the migraine, familial hemiplegic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

migraine, familial hemiplegic Gene Set

From OMIM Gene-Disease Associations

genes associated with the migraine, familial hemiplegic phenotype from the curated OMIM Gene-Disease Associations dataset.

Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bronchiectasis with or without elevated sweat chloride 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bronchiectasis with or without elevated sweat chloride 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Woolly hair, autosomal recessive 2, with or without hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Woolly hair, autosomal recessive 2, with or without hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 7 with or without atrioventricular conduction defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 12 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 12 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy, cystic, without megalencephaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy, cystic, without megalencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cognitive impairment with or without cerebellar ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cognitive impairment with or without cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 19 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 19 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 17 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 17 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, progressive myoclonic 4, with or without renal failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bronchiectasis with or without elevated sweat chloride 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bronchiectasis with or without elevated sweat chloride 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, without vestibular involvement, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, without vestibular involvement, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Testicular anomalies with or without congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Capillary malformation without arteriovenous malformation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Capillary malformation without arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acrodysostosis 2, with or without hormone resistance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acrodysostosis 2, with or without hormone resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 13 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 13 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, with or without seizures, ARX-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, with or without seizures, ARX-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 10 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 10 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adult i Blood Group with or without Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Focal epilepsy with speech disorder with or without mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Focal epilepsy with speech disorder with or without mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 11 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 11 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

IFAP syndrome with or without BRESHECK syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the IFAP syndrome with or without BRESHECK syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency 26 with or without neurologic abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency 26 with or without neurologic abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Goiter, multinodular 1, with or without sertoli-leydig cell tumors Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Goiter, multinodular 1, with or without sertoli-leydig cell tumors phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

H2AX complex, isolated from cells without IR exposure Gene Set

From CORUM Protein Complexes

proteins in the H2AX complex, isolated from cells without IR exposure protein complex from the CORUM Protein Complexes dataset.

DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT from the curated CTD Gene-Disease Associations dataset.

Leukoencephalopathy, Cystic, Without Megalencephaly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukoencephalopathy, Cystic, Without Megalencephaly from the curated CTD Gene-Disease Associations dataset.

NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS from the curated CTD Gene-Disease Associations dataset.

Bronchiectasis With Or Without Elevated Sweat Chloride 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 1 from the curated CTD Gene-Disease Associations dataset.

Bronchiectasis With Or Without Elevated Sweat Chloride 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 2 from the curated CTD Gene-Disease Associations dataset.

Bronchiectasis With Or Without Elevated Sweat Chloride 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 3 from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency without anhidrotic ectodermal dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency without anhidrotic ectodermal dysplasia from the curated CTD Gene-Disease Associations dataset.

HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.

Bifid Nose With Or Without Anorectal And Renal Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset.

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE from the curated CTD Gene-Disease Associations dataset.

Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) from the curated CTD Gene-Disease Associations dataset.

Metaphyseal Dysplasia without Hypotrichosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Metaphyseal Dysplasia without Hypotrichosis from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related from the curated CTD Gene-Disease Associations dataset.

ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.

THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA from the curated CTD Gene-Disease Associations dataset.

Nonmedullary thyroid carcinoma, with or without cell oxyphilia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nonmedullary thyroid carcinoma, with or without cell oxyphilia from the curated CTD Gene-Disease Associations dataset.

SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY from the curated CTD Gene-Disease Associations dataset.

Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia from the curated CTD Gene-Disease Associations dataset.

ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset.

cleft lip with cleft palate; cleft lip without cleft palate; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

salmeterol with or without fluticasone propionate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease salmeterol with or without fluticasone propionate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip with or without cleft palate; cleft palate, isolated Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with or without cleft palate; cleft palate, isolated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip with cleft palate; cleft lip without cleft palate; cleft lip Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate; cleft lip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv; tuberculosis; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv; tuberculosis; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip with or without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nonsyndromic cleft lipor without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nonsyndromic cleft lipor without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip without cleft palate; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip without cleft palate; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital anomalies; cleft lip with or without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital anomalies; cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nonsyndromic cleft lip with or without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nonsyndromic cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

without Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term without in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

cell cycle comprising mitosis without cytokinesis Gene Set

From GO Biological Process Annotations

genes participating in the cell cycle comprising mitosis without cytokinesis biological process from the curated GO Biological Process Annotations dataset.

focal seizures without impairment of consciousness or awareness Gene Set

From HPO Gene-Disease Associations

genes associated with the focal seizures without impairment of consciousness or awareness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 3, with or without intracellular inclusions Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 3, with or without intracellular inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypogonadotropic hypogonadism 15 with or without anosmia} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypogonadotropic hypogonadism 15 with or without anosmia} phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

brain small vessel disease with or without ocular anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the brain small vessel disease with or without ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

paragangliomas 1, with or without deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the paragangliomas 1, with or without deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

metaphyseal dysplasia without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the metaphyseal dysplasia without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 4 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 4 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

central hypoventilation syndrome, congenital, with or without hirschsprung disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the central hypoventilation syndrome, congenital, with or without hirschsprung disease phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 14 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 14 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 2e, with or without neurologic involvement Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 2e, with or without neurologic involvement phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 2, primary, autosomal recessive, with or without cortical malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 2, primary, autosomal recessive, with or without cortical malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

cognitive impairment with or without cerebellar ataxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cognitive impairment with or without cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 6 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 6 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 10 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 10 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 3 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 3 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 8 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 8 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

leukemia, megakaryoblastic, with or without down syndrome, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukemia, megakaryoblastic, with or without down syndrome, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

antley-bixler syndrome without genital anomalies or disordered steroidogenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the antley-bixler syndrome without genital anomalies or disordered steroidogenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 5 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 5 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 7 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 7 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

?microtia with or without hearing impairment (ad) Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microtia with or without hearing impairment (ad) phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, x-linked, with/without neutropenia and/or platelet abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, x-linked, with/without neutropenia and/or platelet abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 11 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 11 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 18 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 18 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

{bronchiectasis with or without elevated sweat chloride 1, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bronchiectasis with or without elevated sweat chloride 1, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

?testicular anomalies with or without congenital heart disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?testicular anomalies with or without congenital heart disease phenotype from the curated OMIM Gene-Disease Associations dataset.

dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema Gene Set

From OMIM Gene-Disease Associations

genes associated with the dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 2 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 2 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

bronchiectasis with or without elevated sweat chloride 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bronchiectasis with or without elevated sweat chloride 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

bronchiectasis with or without elevated sweat chloride 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bronchiectasis with or without elevated sweat chloride 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

bronchiectasis with or without elevated sweat chloride 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bronchiectasis with or without elevated sweat chloride 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 6, autosomal recessive, with or without frontotemporal dementia Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 6, autosomal recessive, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

acrodysostosis 1, with or without hormone resistance Gene Set

From OMIM Gene-Disease Associations

genes associated with the acrodysostosis 1, with or without hormone resistance phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 20 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 20 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

?hypogonadotropic hypogonadism 13 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?hypogonadotropic hypogonadism 13 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.

pulmonary hypertension, familial primary, 1, with or without hht Gene Set

From OMIM Gene-Disease Associations

genes associated with the pulmonary hypertension, familial primary, 1, with or without hht phenotype from the curated OMIM Gene-Disease Associations dataset.

?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

woolly hair, autosomal recessive 1, with or without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the woolly hair, autosomal recessive 1, with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 4 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 4 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

dementia, frontotemporal, with or without parkinsonism Gene Set

From OMIM Gene-Disease Associations

genes associated with the dementia, frontotemporal, with or without parkinsonism phenotype from the curated OMIM Gene-Disease Associations dataset.

leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 9 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 9 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 9 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 9 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 1, with or without congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 1, with or without congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

tooth agenesis, selective, 1, with or without orofacial cleft Gene Set

From OMIM Gene-Disease Associations

genes associated with the tooth agenesis, selective, 1, with or without orofacial cleft phenotype from the curated OMIM Gene-Disease Associations dataset.

?hypogonadotropic hypogonadism 12 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?hypogonadotropic hypogonadism 12 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 6 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 6 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 9, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 9, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract, pulverulent or cerulean, with or without microcornea Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract, pulverulent or cerulean, with or without microcornea phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, x-linked, with or without dyserythropoietic anemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia, x-linked, with or without dyserythropoietic anemia phenotype from the curated OMIM Gene-Disease Associations dataset.

gastric cancer, familial diffuse, with or without cleft lip and/or palate Gene Set

From OMIM Gene-Disease Associations

genes associated with the gastric cancer, familial diffuse, with or without cleft lip and/or palate phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 4, with or without renal failure Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 1 with or without anosmia (kallmann syndrome 1) Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 1 with or without anosmia (kallmann syndrome 1) phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 7, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 7, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

gyrate atrophy of choroid and retina with or without ornithinemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the gyrate atrophy of choroid and retina with or without ornithinemia phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 19 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 19 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, with or without nystagmus Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, with or without nystagmus phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, neurosensory, without vestibular involvement, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, neurosensory, without vestibular involvement, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 14, with or without frontotemporal dementia Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 14, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

adult i phenotype without cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the adult i phenotype without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

leukoencephalopathy, cystic, without megalencephaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy, cystic, without megalencephaly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 8 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 8 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

branchiootorenal syndrome 1, with or without cataracts Gene Set

From OMIM Gene-Disease Associations

genes associated with the branchiootorenal syndrome 1, with or without cataracts phenotype from the curated OMIM Gene-Disease Associations dataset.

mcleod syndrome with or without chronic granulomatous disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the mcleod syndrome with or without chronic granulomatous disease phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 1, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 1, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypogonadotropic hypogonadism 16 with or without anosmia} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypogonadotropic hypogonadism 16 with or without anosmia} phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 7, with or without av conduction defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 7, with or without av conduction defects phenotype from the curated OMIM Gene-Disease Associations dataset.

bifid nose with or without anorectal and renal anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the bifid nose with or without anorectal and renal anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

androgen insensitivity, partial, with or without breast cancer Gene Set

From OMIM Gene-Disease Associations

genes associated with the androgen insensitivity, partial, with or without breast cancer phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 17 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 17 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, focal, with speech disorder and with or without mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, focal, with speech disorder and with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

encephalopathy, progressive, with or without lipodystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopathy, progressive, with or without lipodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 2 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 2 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

woolly hair, autosomal recessive 2 with or without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the woolly hair, autosomal recessive 2 with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

ifap syndrome with or without bresheck syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ifap syndrome with or without bresheck syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertrichosis terminalis, generalized, with or without gingival hyperplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypertrichosis terminalis, generalized, with or without gingival hyperplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency 16, with or without neurologic abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency 16, with or without neurologic abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 5 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 5 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 3, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 3, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

acrodysostosis 2, with or without hormone resistance Gene Set

From OMIM Gene-Disease Associations

genes associated with the acrodysostosis 2, with or without hormone resistance phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperproinsulinemia, familial, with or without diabetes Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperproinsulinemia, familial, with or without diabetes phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 3, with or without dilated cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 3, with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 7 without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 7 without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

anterior segment anomalies with or without cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the anterior segment anomalies with or without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, dopa-responsive, with or without hyperphenylalaninemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, dopa-responsive, with or without hyperphenylalaninemia phenotype from the curated OMIM Gene-Disease Associations dataset.

sweat chloride elevation without cf Gene Set

From OMIM Gene-Disease Associations

genes associated with the sweat chloride elevation without cf phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 15, with or without frontotemporal dementia Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 15, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

?cardiac conduction disease with or without dilated cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cardiac conduction disease with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 10, with or without ftd Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 10, with or without ftd phenotype from the curated OMIM Gene-Disease Associations dataset.

goiter, multinodular 1, with or without sertoli-leydig cell tumors Gene Set

From OMIM Gene-Disease Associations

genes associated with the goiter, multinodular 1, with or without sertoli-leydig cell tumors phenotype from the curated OMIM Gene-Disease Associations dataset.

TG(20:3n6/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

role of brca1 brca2 and atr in cancer susceptibility Gene Set

From Biocarta Pathways

proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.

Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

Malignant hyperthermia susceptibility type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Malignant hyperthermia susceptibility type 2 from the curated CTD Gene-Disease Associations dataset.

Malignant hyperthermia susceptibility type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Malignant hyperthermia susceptibility type 3 from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

Malignant hyperthermia susceptibility type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Malignant hyperthermia susceptibility type 1 from the curated CTD Gene-Disease Associations dataset.

Malignant hyperthermia susceptibility type 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Malignant hyperthermia susceptibility type 6 from the curated CTD Gene-Disease Associations dataset.

MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset.

HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY from the curated CTD Gene-Disease Associations dataset.

SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7 from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5 from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 8 from the curated CTD Gene-Disease Associations dataset.

AUTISM, SUSCEPTIBILITY TO, X-LINKED 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTISM, SUSCEPTIBILITY TO, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset.

ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset.

VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset.

SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 7 from the curated CTD Gene-Disease Associations dataset.

MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8 from the curated CTD Gene-Disease Associations dataset.

ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

SYSTEMIC LUPUS ERYTHEMATOSUS WITH HEMOLYTIC ANEMIA, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SYSTEMIC LUPUS ERYTHEMATOSUS WITH HEMOLYTIC ANEMIA, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset.

AUTISM, SUSCEPTIBILITY TO, X-LINKED 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTISM, SUSCEPTIBILITY TO, X-LINKED 2 from the curated CTD Gene-Disease Associations dataset.

AUTISM, SUSCEPTIBILITY TO, X-LINKED 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTISM, SUSCEPTIBILITY TO, X-LINKED 3 from the curated CTD Gene-Disease Associations dataset.

TOBACCO ADDICTION, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TOBACCO ADDICTION, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION from the curated CTD Gene-Disease Associations dataset.

Malignant hyperthermia susceptibility type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Malignant hyperthermia susceptibility type 4 from the curated CTD Gene-Disease Associations dataset.

Disease Susceptibility Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Disease Susceptibility from the curated CTD Gene-Disease Associations dataset.

DIABETES MELLITUS, INSULIN-DEPENDENT, X-LINKED, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DIABETES MELLITUS, INSULIN-DEPENDENT, X-LINKED, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 from the curated CTD Gene-Disease Associations dataset.

MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 from the curated CTD Gene-Disease Associations dataset.

MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 from the curated CTD Gene-Disease Associations dataset.

MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset.

BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

COXSACKIEVIRUS B3 SUSCEPTIBILITY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease COXSACKIEVIRUS B3 SUSCEPTIBILITY from the curated CTD Gene-Disease Associations dataset.

FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 5 from the curated CTD Gene-Disease Associations dataset.

SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 from the curated CTD Gene-Disease Associations dataset.

GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset.

Malignant hyperthermia susceptibility type 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Malignant hyperthermia susceptibility type 5 from the curated CTD Gene-Disease Associations dataset.

MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5 from the curated CTD Gene-Disease Associations dataset.

MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

OROFACIAL CLEFT 6, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OROFACIAL CLEFT 6, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 6 from the curated CTD Gene-Disease Associations dataset.

GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

NEPHROLITHIASIS, URIC ACID, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEPHROLITHIASIS, URIC ACID, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

vitiligo susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vitiligo susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; atherosclerosis; disease susceptibility; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; atherosclerosis; disease susceptibility; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; disease susceptibility; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet syndrome; disease susceptibility; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

prion susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease prion susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lung cancer susceptibility and prognosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung cancer susceptibility and prognosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; disease susceptibility; gastrointestinal neoplasms; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; disease susceptibility; gastrointestinal neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

burns; disease susceptibility; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease burns; disease susceptibility; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atopy-susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atopy-susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

susceptibility to multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease susceptibility to multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; autoimmune diseases; disease susceptibility; lupus erythematosus, systemic; rheumatoid arthritis; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; autoimmune diseases; disease susceptibility; lupus erythematosus, systemic; rheumatoid arthritis; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute coronary syndrome; alveolar bone loss; angina pectoris; disease susceptibility; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; alveolar bone loss; angina pectoris; disease susceptibility; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dental plaque; disease susceptibility; gingivitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dental plaque; disease susceptibility; gingivitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; disease susceptibility; pseudomonas infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; disease susceptibility; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cancer susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cancer susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; disease susceptibility; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; disease susceptibility; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

susceptibility to tuberculosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease susceptibility to tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; disease susceptibility; polyendocrinopathies, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; disease susceptibility; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disease susceptibility; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disease susceptibility; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

altitude sickness; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease altitude sickness; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

susceptibility to visceral leishmaniasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease susceptibility to visceral leishmaniasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; disease susceptibility; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; disease susceptibility; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lung cancer susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung cancer susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

susceptibility to hiv-1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease susceptibility to hiv-1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacterial infections; disease susceptibility; lupus erythematosus, systemic; opportunistic infections; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial infections; disease susceptibility; lupus erythematosus, systemic; opportunistic infections; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aspergillosis; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aspergillosis; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

susceptibility to autoimmune disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease susceptibility to autoimmune disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic ketoacidosis; disease susceptibility; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic ketoacidosis; disease susceptibility; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma; disease susceptibility; endometrial neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma; disease susceptibility; endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; aplastic anemia; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; aplastic anemia; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ovalocytosis and malaria susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ovalocytosis and malaria susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

susceptibility to lead Gene Set

From GAD Gene-Disease Associations

genes associated with the disease susceptibility to lead in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cancer predisposition and susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cancer predisposition and susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angioedema; disease susceptibility; urticaria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angioedema; disease susceptibility; urticaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic aneurysm, abdominal; disease susceptibility; hypertension; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic aneurysm, abdominal; disease susceptibility; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hereditary and sporadic prostate cancer susceptibility. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary and sporadic prostate cancer susceptibility. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

septic shock susceptibility & mortality Gene Set

From GAD Gene-Disease Associations

genes associated with the disease septic shock susceptibility & mortality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

manganism, susceptibility to occupational chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease manganism, susceptibility to occupational chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

septic shock (susceptibility & mortality) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease septic shock (susceptibility & mortality) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchiolitis; disease susceptibility; respiratory syncytial virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchiolitis; disease susceptibility; respiratory syncytial virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dementia; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast cancer susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast cancer susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disease susceptibility; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disease susceptibility; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

communicable diseases; disease susceptibility; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease communicable diseases; disease susceptibility; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

susceptibility Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term susceptibility in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

susceptibility to t cell mediated cytotoxicity Gene Set

From GO Biological Process Annotations

genes participating in the susceptibility to t cell mediated cytotoxicity biological process from the curated GO Biological Process Annotations dataset.

susceptibility to natural killer cell mediated cytotoxicity Gene Set

From GO Biological Process Annotations

genes participating in the susceptibility to natural killer cell mediated cytotoxicity biological process from the curated GO Biological Process Annotations dataset.

HIV-1 susceptibility Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the HIV-1 susceptibility phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

susceptibility to chickenpox Gene Set

From HPO Gene-Disease Associations

genes associated with the susceptibility to chickenpox phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bruising susceptibility Gene Set

From HPO Gene-Disease Associations

genes associated with the bruising susceptibility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

susceptibility to herpesvirus Gene Set

From HPO Gene-Disease Associations

genes associated with the susceptibility to herpesvirus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased susceptibility to fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the increased susceptibility to fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Disease Susceptibility Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Disease Susceptibility phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Susceptibility to monomelic amyotrophy Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Susceptibility to monomelic amyotrophy protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Breast cancer type 1 susceptibility protein (BRCA1) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Breast cancer type 1 susceptibility protein (BRCA1) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Psoriasis susceptibility 1 candidate gene 2 protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Psoriasis susceptibility 1 candidate gene 2 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Breast cancer type 2 susceptibility protein, helical domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Breast cancer type 2 susceptibility protein, helical domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Autism susceptibility gene 2 protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Autism susceptibility gene 2 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Breast cancer type 2 susceptibility protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Breast cancer type 2 susceptibility protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cancer susceptibility candidate 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cancer susceptibility candidate 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Psoriasis susceptibility 1 candidate 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Psoriasis susceptibility 1 candidate 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cancer susceptibility candidate protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cancer susceptibility candidate protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

decreased susceptibility to viral infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to viral infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to systemic lupus erythematosus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to systemic lupus erythematosus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to kidney reperfusion injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to kidney reperfusion injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to neuronal excitotoxicity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to neuronal excitotoxicity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to bacterial infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to bacterial infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced joint inflammation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced joint inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to parasitic infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to parasitic infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to atherosclerosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to atherosclerosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to type i hypersensitivity reaction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to type i hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to experimental autoimmune uveoretinitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to experimental autoimmune uveoretinitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to autoimmune diabetes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to autoimmune diabetes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to autoimmune disorder Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to autoimmune disorder phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to kidney reperfusion injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to kidney reperfusion injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced choroid neovascularization Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced choroid neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to autoimmune disorder Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to autoimmune disorder phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to ototoxicity-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to ototoxicity-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to bone fracture Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to bone fracture phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to bacterial infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to bacterial infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered tumor susceptibility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered tumor susceptibility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to dystrophic cardiac calcinosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to dystrophic cardiac calcinosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induction of seizure by inducing agent Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induction of seizure by inducing agent phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to weight loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to type ii hypersensitivity reaction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to type ii hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to weight gain Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to weight gain phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to parasitic infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to parasitic infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to experimental autoimmune myasthenia gravis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to experimental autoimmune myasthenia gravis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to experimental autoimmune myasthenia gravis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to experimental autoimmune myasthenia gravis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to experimental autoimmune uveoretinitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to experimental autoimmune uveoretinitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to bacterial infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to bacterial infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to atherosclerosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to atherosclerosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to atherosclerosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to atherosclerosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced pancreatitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced pancreatitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to dopaminergic neuron neurotoxicity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to dopaminergic neuron neurotoxicity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to viral infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to viral infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to neuronal excitotoxicity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to neuronal excitotoxicity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to osteoporosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to osteoporosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to weight loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to age related obesity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to age related obesity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to osteoporosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to osteoporosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to age related obesity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to age related obesity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to type iii hypersensitivity reaction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to type iii hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to viral infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to viral infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to age-related hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to age-related hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to bacterial infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to bacterial infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to dopaminergic neuron neurotoxicity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to dopaminergic neuron neurotoxicity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to autoimmune hemolytic anemia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to autoimmune hemolytic anemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to otitis media Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to otitis media phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to fungal infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to fungal infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced colitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced colitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to viral infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to viral infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to prion infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to prion infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to weight gain Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to weight gain phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to type iv hypersensitivity reaction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to type iv hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to autoimmune diabetes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to autoimmune diabetes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to autoimmune disorder Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to autoimmune disorder phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced colitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced colitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to experimental autoimmune encephalomyelitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to experimental autoimmune encephalomyelitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to hyperlipidemia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to hyperlipidemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced arthritis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced arthritis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to noise-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to parasitic infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to parasitic infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to systemic lupus erythematosus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to systemic lupus erythematosus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to parasitic infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to parasitic infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to ischemic brain injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to ischemic brain injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to pharmacologically induced seizures Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to pharmacologically induced seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to bacterial infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to bacterial infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced retinal damage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced retinal damage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced pancreatitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced pancreatitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to dystrophic cardiac calcinosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to dystrophic cardiac calcinosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to graft versus host disease Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to graft versus host disease phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to type iii hypersensitivity reaction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to type iii hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to autoimmune hemolytic anemia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to autoimmune hemolytic anemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to type iv hypersensitivity reaction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to type iv hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to experimental autoimmune encephalomyelitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to experimental autoimmune encephalomyelitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to fungal infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to fungal infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to diet-induced obesity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to diet-induced obesity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to graft versus host disease Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to graft versus host disease phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to viral infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to viral infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to fungal infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to fungal infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced choroidal neovascularization Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced choroidal neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to parasitic infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to parasitic infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced arthritis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced arthritis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to noise-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal susceptibility to weight loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to prion infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to prion infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to diet-induced obesity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to diet-induced obesity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to endotoxin shock Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to endotoxin shock phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to pharmacologically induced seizures Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to pharmacologically induced seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to kidney reperfusion injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to kidney reperfusion injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to endotoxin shock Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to endotoxin shock phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to type i hypersensitivity reaction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to type i hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to ischemic brain injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to ischemic brain injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induction of seizure by inducing agent Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induction of seizure by inducing agent phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal susceptibility to induced colitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal susceptibility to induced colitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to prion infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to prion infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal susceptibility to hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal susceptibility to hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to hepatic steatosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to hepatic steatosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal susceptibility to weight gain Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal susceptibility to weight gain phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{encephalopathy, acute, infection-induced, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {encephalopathy, acute, infection-induced, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{sublingual nitroglycerin, susceptibility to poor response to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {sublingual nitroglycerin, susceptibility to poor response to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{systemic lupus erythematous, association with susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {systemic lupus erythematous, association with susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{autoimmune disease, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autoimmune disease, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{low renin hypertension, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {low renin hypertension, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{autism, susceptibility to, x-linked 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autism, susceptibility to, x-linked 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{nasopharyngeal carcinoma, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {nasopharyngeal carcinoma, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pelvic organ prolapse, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pelvic organ prolapse, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pancreatic cancer, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pancreatic cancer, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pregnancy loss, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pregnancy loss, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pulmonary disease, chronic obstructive, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pulmonary disease, chronic obstructive, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{malaria, cerebral, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {malaria, cerebral, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{malignant hyperthermia susceptibility 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {malignant hyperthermia susceptibility 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{colon cancer, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {colon cancer, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pemphigoid, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pemphigoid, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{systemic lupus erythematosus susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {systemic lupus erythematosus susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{spina bifida, folate-sensitive, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {spina bifida, folate-sensitive, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{malaria, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {malaria, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary artery spasm 2, susceptibility to Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary artery spasm 2, susceptibility to phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, idiopathic generalized, susceptibility to, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, idiopathic generalized, susceptibility to, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

{craniosynostosis 5, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {craniosynostosis 5, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{lupus nephritis, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {lupus nephritis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{sarcoidosis, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {sarcoidosis, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{patent ductus arteriosus, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {patent ductus arteriosus, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hepatic fibrosis susceptibility due to schistosoma mansoni infection} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hepatic fibrosis susceptibility due to schistosoma mansoni infection} phenotype from the curated OMIM Gene-Disease Associations dataset.

{asthma, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {asthma, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{autoimmune disease, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autoimmune disease, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{dyslexia, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {dyslexia, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{asthma susceptibility 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {asthma susceptibility 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{autism susceptibility 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autism susceptibility 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{leukemia, acute myeloid, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {leukemia, acute myeloid, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pancreatic cancer, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pancreatic cancer, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{systemic lupus erythematosus, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {systemic lupus erythematosus, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{basal cell carcinoma, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {basal cell carcinoma, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

herpes simplex encephalitis, susceptibility to, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the herpes simplex encephalitis, susceptibility to, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

{malignant hyperthermia susceptibility 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {malignant hyperthermia susceptibility 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, susceptibility to, bmiq11} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, susceptibility to, bmiq11} phenotype from the curated OMIM Gene-Disease Associations dataset.

{colorectal cancer, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {colorectal cancer, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{asthma, nocturnal, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {asthma, nocturnal, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{glioma susceptibility 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {glioma susceptibility 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{fibrocalculous pancreatic diabetes, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {fibrocalculous pancreatic diabetes, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{spondyloarthropathy, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {spondyloarthropathy, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hirschsprung disease, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hirschsprung disease, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{dermatitis, atopic, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {dermatitis, atopic, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{autoimmune disease, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autoimmune disease, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{dyslexia, susceptibility to, 8} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {dyslexia, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.

{sepsis, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {sepsis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypertension, essential, susceptibility to, 7} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypertension, essential, susceptibility to, 7} phenotype from the curated OMIM Gene-Disease Associations dataset.

{basal cell carcinoma, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {basal cell carcinoma, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{autoimmune thyroid disease, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autoimmune thyroid disease, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{malignant hyperthermia susceptibility 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {malignant hyperthermia susceptibility 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{benzene toxicity, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {benzene toxicity, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{colorectal cancer, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {colorectal cancer, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{glioma susceptibility 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {glioma susceptibility 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{allergic rhinitis, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {allergic rhinitis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{dermatitis, atopic, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {dermatitis, atopic, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{prostate cancer, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {prostate cancer, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{prostate cancer, hereditary, 2, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {prostate cancer, hereditary, 2, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypertension, essential, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypertension, essential, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{osteoporosis, early-onset, susceptibility to, autosomal dominant} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {osteoporosis, early-onset, susceptibility to, autosomal dominant} phenotype from the curated OMIM Gene-Disease Associations dataset.

{thyrotoxic periodic paralysis, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {thyrotoxic periodic paralysis, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{asthma, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {asthma, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypertriglyceridemia, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypertriglyceridemia, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{aspergillosis, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {aspergillosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{breast cancer, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {breast cancer, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{basal cell carcinoma, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {basal cell carcinoma, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stevens-johnson syndrome, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stevens-johnson syndrome, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary heart disease, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary heart disease, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{colorectal cancer, susceptibility to, 7} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {colorectal cancer, susceptibility to, 7} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile myoclonic, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile myoclonic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{major affective disorder-8, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {major affective disorder-8, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{atrioventricular septal defect, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {atrioventricular septal defect, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{glaucoma, normal tension, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {glaucoma, normal tension, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{otitis media, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {otitis media, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hodgkin lymphoma, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hodgkin lymphoma, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{dermatitis, atopic, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {dermatitis, atopic, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{colorectal cancer, susceptibility to, 11} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {colorectal cancer, susceptibility to, 11} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hepatitis b virus, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hepatitis b virus, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{lung cancer susceptibility 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {lung cancer susceptibility 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypertension, essential, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypertension, essential, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{preeclampsia, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {preeclampsia, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{autism susceptibility 8} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autism susceptibility 8} phenotype from the curated OMIM Gene-Disease Associations dataset.

{systemic lupus erythematosus, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {systemic lupus erythematosus, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{anorexia nervosa, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {anorexia nervosa, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{scoliosis, idiopathic, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {scoliosis, idiopathic, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{encephalopathy, acute, infection-induced, 3, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {encephalopathy, acute, infection-induced, 3, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary heart disease, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary heart disease, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{seasonal affective disorder, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {seasonal affective disorder, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{colorectal cancer, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {colorectal cancer, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{autism susceptibility, x-linked 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autism susceptibility, x-linked 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{graves disease, susceptibility to, x-linked} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {graves disease, susceptibility to, x-linked} phenotype from the curated OMIM Gene-Disease Associations dataset.

{glioma susceptibility 8} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {glioma susceptibility 8} phenotype from the curated OMIM Gene-Disease Associations dataset.

{lewy body dementia, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {lewy body dementia, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pseudofolliculitis barbae, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pseudofolliculitis barbae, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hirschsprung disease, susceptibility to, 8} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hirschsprung disease, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.

{psoraisis susceptibility 9} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {psoraisis susceptibility 9} phenotype from the curated OMIM Gene-Disease Associations dataset.

{colorectal cancer, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {colorectal cancer, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{dermatitis, atopic, susceptibility to, 7} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {dermatitis, atopic, susceptibility to, 7} phenotype from the curated OMIM Gene-Disease Associations dataset.

{neural tube defects, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {neural tube defects, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple myeloma, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple myeloma, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{kala-azar, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {kala-azar, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypertension, essential, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypertension, essential, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pelvic organ prolapse, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pelvic organ prolapse, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{breast cancer, male, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {breast cancer, male, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{osteoarthritis susceptibility 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {osteoarthritis susceptibility 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{opioid dependence, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {opioid dependence, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{kawasaki disease, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {kawasaki disease, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{systemic lupus erythematosus, susceptibility to, 12} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {systemic lupus erythematosus, susceptibility to, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.

{nephrolithiasis, uric acid, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {nephrolithiasis, uric acid, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary heart disease, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary heart disease, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{malaria, mild, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {malaria, mild, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{myocardial infarction, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {myocardial infarction, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{psoriasis susceptibility 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {psoriasis susceptibility 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{memory impairment, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {memory impairment, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{osteoporosis, postmenopausal, susceptibility} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {osteoporosis, postmenopausal, susceptibility} phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, susceptibility to, bmiq8} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, susceptibility to, bmiq8} phenotype from the curated OMIM Gene-Disease Associations dataset.

{parkinson disease, late-onset, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {parkinson disease, late-onset, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

?{autism susceptibility 16} Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?{autism susceptibility 16} phenotype from the curated OMIM Gene-Disease Associations dataset.

{attention deficit-hyperactivity disorder, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {attention deficit-hyperactivity disorder, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{?schizophrenia, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {?schizophrenia, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{nonsmall cell lung cancer, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {nonsmall cell lung cancer, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.