- OMIM ID
-
147950
- OMIM term:
- KALLMANN SYNDROME 2; KAL2
- Alternative terms:
-
HYPOGONADOTROPIC HYPOGONADISM AND ANOSMIA KALLMANN SYNDROME 2 WITH CLEFT LIP OR PALATE, INCLUDED
KALLMANN SYNDROME 2 WITH BIMANUAL SYNKINESIA, INCLUDED
KALLMANN SYNDROME 2 WITH SELECTIVE TOOTH AGENESIS, INCLUDED
- (∗) Location:
- 8p11.23-p11.22
- (†) Associated OMIM genes:
- FGFR1
- (‡) Associated MGI genes:
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