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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: Endocrine System Diseases (D004700)
Parent Node: Hypothalamic Diseases (D007027)
..Starting node ..Pituitary Diseases (D010900)
Child 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
Sister Nodes:
..Bardet-Biedl Syndrome (D020788) 13
..Hypothalamic hamartomas (C537158)
..Hypothalamic Neoplasms (D007029) 7
..Laurence-Moon Syndrome (D007849)
..Microgastria limb reduction defect (C537554)
..Pituitary Diseases (D010900) 60
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8958
Name:	Pituitary Diseases
Definition:	Disorders involving either the ADENOHYPOPHYSIS or the NEUROHYPOPHYSIS. These diseases usually manifest as hypersecretion or hyposecretion of PITUITARY HORMONES. Neoplastic pituitary masses can also cause compression of the OPTIC CHIASM and other adjacent structures.
Alternative IDs:
ParentIDs:	MESH:D004700\|MESH:D007027
TreeNumbers:	C10.228.140.617.738 \|C19.700
Synonyms:	Adenohypophyseal Disease \|Adenohypophyseal Diseases \|Anterior Pituitary Disease \|Anterior Pituitary Diseases \|Disease, Adenohypophyseal \|Disease, Anterior Pituitary \|Disease, Neurohypophyseal \|Disease, Pituitary \|Disease, Pituitary Gland \|Disease, Posterior Pitui
Slim Mappings:	Endocrine system disease\|Nervous system disease
Reference:	MedGen: D010900 MeSH: D010900 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants