(Q32038861)
English
hypogonadotropic hypogonadism 6 with or without anosmia
hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has material basis in heterozygous mutation in the FGF8 gene on chromosome 10q24, sometimes in association with mutation in another gene
- Kallmann syndrome 6
- HH6
- KAL6
- HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA
- HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA; HH6
Statements
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Identifiers
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