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Combined Pituitary Hormone Deficiency MeSH Supplementary Concept Data 2023


MeSH Supplementary
Combined Pituitary Hormone Deficiency
Unique ID
C580003
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C580003
Entry Term(s)
Panhypopituitarism
Registry Number
0
Heading Mapped to
*Hypopituitarism
Frequency
305
Note
A hereditary autosomal recessive form of hypopituitarism that is characterized by growth retardation, HYPOTHYROIDISM, reduced levels of CORTISOL, and absent or DELAYED PUBERTY due to low levels of LUTEINIZING HORMONE or FOLLICLE-STIMULATING HORMONE . Rarely, INTELLECTUAL DISABILITY, neck abnormalities, and OPTIC NERVE defects may also occur. Mutations in the PROP1 gene have been identified in some cases. OMIM: 262600
Date of Entry
2013/10/24
Revision Date
2015/08/18
Combined Pituitary Hormone Deficiency Preferred
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