Pituitary Hormone Deficiency, Combined, 2 (CPHD2)

Alias:
Panhypopituitarism
Combined Pituitary Hormone Deficiency
Ateliotic Dwarfism with Hypogonadism
Pituitary Dwarfism Iii
Hanhart Dwarfism
Cphd2
Hormone Deficiency, Pituitary, Combined, Type 2
Hormone Deficiency, Pituitary, Combined
Pituitary Hormone Deficiency, Combined
Pituitary Dwarfism Type 3
Simmond's Disease
Simmonds' Disease
Sheehan Syndrome
Cphd
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Pituitary Hormone Deficiency, Combined, 2, also known as panhypopituitarism, is related to panhypopituitarism, x-linked and pituitary hormone deficiency, combined or isolated, 1. An important gene associated with Pituitary Hormone Deficiency, Combined, 2 is PROP1 (PROP Paired-Like Homeobox 1), and among its related pathways/superpathways are Class A/1 (Rhodopsin-like receptors) and Signal Transduction. The drugs Oxytocin and Exenatide have been mentioned in the context of this disorder. Affiliated tissues include pituitary and thyroid, and related phenotypes are reduced circulating prolactin concentration and decreased circulating luteinizing hormone level
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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32
327
65

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
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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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