Term Name: combined pituitary hormone deficiency 2
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.
Ontology: Human Disease [DOID:0061020]   ( DOID:0061020 )

Relationships
is a type of: autosomal recessive disease combined pituitary hormone deficiency