FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term combined or isolated pituitary hormone deficiency 8 ID (Ontology) DOID:0061018 (Human Disease)
Definition A combined pituitary hormone deficiency that has_material_basis_in heterozygous mutation in the ROBO1 gene on chromosome 3p12.
Also Known As "CPHD8"
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 combined or isolated pituitary hormone deficiency 8       3
 for disease ribbon | combined or isolated pituitary hormone deficiency 8       3
 model of | combined or isolated pituitary hormone deficiency 8       3
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_____________
hypopituitarism                            |
 |__combined pituitary hormone deficiency__|
                                           combined or isolated pituitary hormone deficiency 8  3 rec.
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Is a autosomal dominant disease
combined pituitary hormone deficiency
Part of
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Synonyms
  • "CPHD8" EXACT OMO:0003012
Secondary IDs
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MIM:620303