Search Ontology:
Human Disease

combined pituitary hormone deficiency 2

Term ID
DOID:0061020
Synonyms
  • CPHD2
Definition
A combined pituitary hormone deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the PROP1 gene on chromosome 5q35. https://pubmed.ncbi.nlm.nih.gov/9462743/
References
Ontology
Human Disease   ( DOID:0061020 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
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