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Disease Ontology Browser
hand-foot-genital syndrome (DOID:0060739)
Alliance: disease page
Synonyms: hand-foot-uterus syndrome; HFGS
Alt IDs: OMIM:140000, ICD10CM:Q51.2, ORDO:2438
Definition: A autosomal dominant disease characterized by distal limb defects (short thumbs and first toes, clinodactyly of the fifth fingers, delayed ossification of the wrist and ankle bones), urogenital defects and that has_material_basis_in heterozygous mutation in the HOXA13 gene on chromosome 7p15.

Disease References using Mouse Models (5)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory