OBO ID: DOID:0090084
Term Name: hypogonadotropic hypogonadism 5 with or without anosmia Search Ontology:
Synonyms:
Definition: A hypogonadotropic hypogonadism that is characterised 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)
OTHER hypogonadotropic hypogonadism 5 with or without anosmia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CHD7 Hypogonadotropic hypogonadism 5 with or without anosmia 612370
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None