(Q32038857)
English
hypogonadotropic hypogonadism 5 with or without anosmia
hypogonadotropic hypogonadism that is characterised by autosomal dominant inheritance and has material basis in heterozygous mutation in the CHD7 gene on chromosome 8q12
- KAL5
- HH5
- HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA; HH5
- HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA
- Kallmann syndrome 5
Statements
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Identifiers
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