Combined Pituitary Hormone Deficiencies, Genetic Forms

Alias:
Multiple Pituitary Hormone Deficiencies, Genetic Forms
Combined Pituitary Hormone Deficiencies, Genetic Form
Familial Congenital Hypopituitarism
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Combined Pituitary Hormone Deficiencies, Genetic Forms, also known as multiple pituitary hormone deficiencies, genetic forms, is related to hypopituitarism and pituitary hormone deficiency, combined, 2. An important gene associated with Combined Pituitary Hormone Deficiencies, Genetic Forms is PROP1 (PROP Paired-Like Homeobox 1), and among its related pathways/superpathways are Embryonic and Induced Pluripotent Stem Cells and Lineage-specific Markers and Endoderm differentiation. Affiliated tissues include pituitary and eye, and related phenotypes are hypopituitarism and hypotension
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XLD
AD
AR
XL
All ages
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7
109
21

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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