Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 7 with or without anosmia
rareA hypogonadotropic hypogonadism that has material basis in homozygous or compound heterozygous mutation in the GNRHR gene on chromosome 4q13, sometimes in association with mutation in another gene. No patients with anosmia have been reported.
- Identifiers
- MONDO:0007794 OMIM:146110
- Causal genes
- GNRHR
- Also known as
- HH7 · hypogonadotropic hypogonadism 7 without anosmia
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