articulation disorder Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A speech disorder that involves mispronouncing speech sounds by omitting, distorting, substituting, or adding sounds which can make speech difficult to understand. (Human Disease Ontology, DOID_4186)
Similar Terms
Downloads & Tools

Genes

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

Symbol Name Standardized Value
ZNF280D zinc finger protein 280D 2.10376
ELP4 elongator acetyltransferase complex subunit 4 1.54451
EPGN epithelial mitogen 1.50623
SMCP sperm mitochondria-associated cysteine-rich protein 1.36291
KIAA0319 KIAA0319 1.30052
DYX1C1 dyslexia susceptibility 1 candidate 1 1.29003
TCF12 transcription factor 12 1.2813
ROBO1 roundabout, axon guidance receptor, homolog 1 (Drosophila) 1.13755
CNTNAP2 contactin associated protein-like 2 1.07362
ITPA inosine triphosphatase (nucleoside triphosphate pyrophosphatase) 1.00414
TBX1 T-box 1 1.00203
FOXP2 forkhead box P2 0.739894
PHGDH phosphoglycerate dehydrogenase 0.420266