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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Pituitary Diseases (D010900)
..Starting node ..Hypopituitarism (D007018)
Child Nodes:
........Arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies (C535385)
........Combined Pituitary Hormone Deficiency (C580003)
........Dincsoy Salih Patel syndrome (C536177)
........Dwarfism, Pituitary (D004393) 11
........Holoprosencephaly 9 (C563659)
........Hypopituitarism and septooptic 'dysplasia' (C531815)
........Hypopituitarism, Congenital, with Central Diabetes Insipidus (C565477)
........Kaplowitz Bodurtha syndrome (C536893)
........Mental Retardation, X-Linked, With Panhypopituitarism (C567485)
........Panhypopituitarism X-linked (C538613)
........Prolactin Deficiency with Obesity and Enlarged Testes (C564870)
........RHYNS syndrome (C537612)
Sister Nodes:
..Diabetes Insipidus (D003919) 10
..Empty Sella Syndrome (D004652) 1
..Hyperpituitarism (D006964) 13
..Hypopituitarism (D007018) 23
..Inappropriate ADH Syndrome (D007177) 1
..Isolated Growth Hormone Deficiency, Type IB (C567564)
..Pituitary Apoplexy (D010899)
..Pituitary Neoplasms (D010911) 5
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5613
Name:	Hypopituitarism
Definition:	Diminution or cessation of secretion of one or more hormones from the anterior pituitary gland (including LH; FOLLICLE STIMULATING HORMONE; SOMATOTROPIN; and CORTICOTROPIN). This may result from surgical or radiation ablation, non-secretory PITUITARY NEOPLASMS, metastatic tumors, infarction, PITUITARY APOPLEXY, infiltrative or granulomatous processes, and other conditions.
Alternative IDs:
ParentIDs:	MESH:D010900
TreeNumbers:	C10.228.140.617.738.300 \|C19.700.482
Synonyms:	Adenohypophyseal Hyposecretion \|Anterior Pituitary Hyposecretion Syndrome \|Disease, Simmonds \|Hypopituitarism, Postpartum \|Hyposecretion, Adenohypophyseal \|Hyposecretion Syndrome, Anterior Pituitary \|Insufficiency, Pituitary \|Panhypopituitarism, Postpartum \|Pitu
Slim Mappings:	Endocrine system disease\|Nervous system disease
Reference:	MedGen: D007018 MeSH: D007018 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants