|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An osteosclerosis that has_material_basis_in mutations in the ANKH gene which results_in progressive thickening located_in skull and abnormally shaped ends of long bones in the limbs. (Human Disease Ontology, DOID_0080033)|
|Downloads & Tools|
1 genes associated with the craniometaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
|ANKH||ANKH inorganic pyrophosphate transport regulator|