Search Ontology:
Human Disease

hypogonadotropic hypogonadism 5 with or without anosmia

Term ID
DOID:0090084
Synonyms
Definition
A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the CHD7 gene on chromosome 8q12. https://www.ncbi.nlm.nih.gov/pubmed/18834967
References
Ontology
Human Disease   ( DOID:0090084 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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