panhypopituitarism

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Information
Disease name
panhypopituitarism
Disease ID
DOID:9410
Description
"A hypopituitarism characterized by deficiency in growth hormone and at least one other pituitary hormone." [url:https\://www.ncbi.nlm.nih.gov/pubmed/27828722]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT00373386 Completed Phase 4 Growth Hormone and Endothelial Function in Children January 2005 December 2007
NCT00144391 Completed Phase 4 Testosterone Gel Applied to Women With Pituitary Gland Problems July 2003 December 2010
NCT04902235 Completed Phase 4 Identification and Clinical Relevance of an Oxytocin Deficient State (CRH Study) July 6, 2021 May 1, 2023
NCT00001595 Recruiting An Investigation of Pituitary Tumors and Related Hypothalmic Disorders April 21, 1997
NCT04897802 Recruiting Phase 4 Identification and Clinical Relevance of an Oxytocin Deficient State (GLP1 Study) September 13, 2021 December 31, 2024
NCT06217848 Recruiting Early Phase 1 The Effect of GLP-1 Agonist in Patients With Hypothalamic Obesity: Prospective, Pilot Study November 28, 2022 March 8, 2024
NCT00144404 Withdrawn Baseline Sexual Function, Cognitive Function, Body Composition and Muscle Parameters and Pharmacokinetics of Transdermal Testosterone Gel in Women With Hypopituitarism August 2002 August 2002
Disase is a (Disease Ontology)
DOID:9406
Cross Reference ID (Disease Ontology)
ICD10CM:E23.0
Cross Reference ID (Disease Ontology)
ICD9CM:253.2
Cross Reference ID (Disease Ontology)
MESH:C580003
Cross Reference ID (Disease Ontology)
MIM:PS613038
Cross Reference ID (Disease Ontology)
NCI:C110940
Cross Reference ID (Disease Ontology)
ORDO:90695
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:154700009
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0242343
Exact Synonym (Disease Ontology)
combined pituitary hormone deficiency
Exact Synonym (Disease Ontology)
Simmond's disease
Exact Synonym (Disease Ontology)
Simmonds' disease
HPO Human Phenotype ID (Human Phenotype Ontology)
HP:0000871