- OMIM ID
-
109120
- OMIM term:
- AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES
- Alternative terms:
-
DE HAUWERE SYNDROME
IRIS DYSPLASIA WITH OCULAR HYPERTELORISM, PSYCHOMOTOR RETARDATION, AND SENSORINEURAL DEAFNESS
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
Loading mouse genes ...