Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 21 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FLRT3 gene.
- Identifiers
- MONDO:0014107 OMIM:615271
- Causal genes
- FLRT3
- Part of
- Kallmann syndrome
- Also known as
- FLRT3 hypogonadotropic hypogonadism · HH21 · hypogonadotropic hypogonadism 21 with anosmia · hypogonadotropic hypogonadism caused by mutation in FLRT3
Projects
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