- OMIM ID
-
307150
- OMIM term:
- HYPERTRICHOSIS, CONGENITAL GENERALIZED; HTC2
- Alternative terms:
-
CHROMOSOME Xq27.1 INTERCHROMOSOMAL INSERTION SYNDROME
CGH
HCG
- (∗) Location:
- Xq27.1
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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