Term Name: | otospondylomegaepiphyseal dysplasia, autosomal recessive |
---|---|
Synonyms: | CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS, NANCE-INSLEY SYNDROME, NANCE-SWEENEY CHONDRODYSPLASIA, OSMEDB |
Definition: | An osteochondrodysplasia that results from mutations autosomal recessive inheritance of mutations in the COL11A2 gene which results_in enlargement of the located_in epiphysis in located_in hand and located_in foot, distinct facial features, platyspondyly and hearing loss. |
Ontology: | Human Disease [DOID:0080026] ( DOID:0080026 ) |