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DO Term : combined or isolated pituitary hormone deficiency 1 [DOID:0061019] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A combined pituitary hormone deficiency that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the POU1F1 gene on chromosome 3p11.
  • synonyms:
  • OMIM:613038,
  • CPHD1,
  • 613038
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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