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| Term | combined pituitary hormone deficiency 2 | ID (Ontology) | DOID:0061020 (Human Disease) |
| Definition | A combined pituitary hormone deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the PROP1 gene on chromosome 5q35. | ||
| Also Known As | "CPHD2" | ||
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autosomal genetic disease |__autosomal recessive disease____________ hypopituitarism | |__combined pituitary hormone deficiency__| combined pituitary hormone deficiency 2 |
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| Is a |
autosomal recessive disease combined pituitary hormone deficiency |
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External Crossreferences & Linkouts
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| MIM:262600 | |||