- OMIM ID
-
166600
- OMIM term:
- OSTEOPETROSIS, AUTOSOMAL DOMINANT 2; OPTA2
- Alternative terms:
-
OSTEOPETROSIS, AUTOSOMAL DOMINANT, TYPE II
MARBLE BONES, AUTOSOMAL DOMINANT
OSTEOSCLEROSIS FRAGILIS GENERALISATA
ALBERS-SCHONBERG DISEASE, AUTOSOMAL DOMINANT
- (∗) Location:
- 16p13.3
- (†) Associated OMIM genes:
- CLCN7
- (‡) Associated MGI genes:
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