- OMIM ID
-
238320
- OMIM term:
- LEYDIG CELL HYPOPLASIA, TYPE I
- Alternative terms:
-
LEYDIG CELL HYPOPLASIA WITH MALE PSEUDOHERMAPHRODITISM
LEYDIG CELL HYPOPLASIA, COMPLETE
LEYDIG CELL AGENESIS LEYDIG CELL HYPOPLASIA, TYPE II, INCLUDED
LEYDIG CELL HYPOPLASIA, PARTIAL, INCLUDED
HYPERGONADOTROPIC HYPOGONADISM, MALE, DUE TO LHCGR DEFECT, INCLUDED
LUTEINIZING HORMONE RESISTANCE, FEMALE, INCLUDED
- (∗) Location:
- 2p16.3
- (†) Associated OMIM genes:
- LHCGR
- (‡) Associated MGI genes:
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