Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 5 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the CHD7 gene.
- Identifiers
- MONDO:0012880 OMIM:612370
- Causal genes
- CHD7
- Part of
- Kallmann syndrome
- Also known as
- CHD7 hypogonadotropic hypogonadism · HH5 · hypogonadotropic hypogonadism caused by mutation in CHD7 · Kallmann syndrome 5
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