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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: Diabetes Mellitus, Type 2 (D003924)
..Starting node ..Diabetes Mellitus, Type II, Autosomal Dominant (C562773)
Child Nodes:
Sister Nodes:
..Diabetes Mellitus, Lipoatrophic (D003923) 1
..Diabetes Mellitus, Noninsulin-Dependent, 1 (C563359)
..Diabetes Mellitus, Noninsulin-Dependent, 2 (C563323)
..Diabetes Mellitus, Noninsulin-Dependent, 3 (C566342)
..Diabetes Mellitus, Noninsulin-Dependent, Type 4 (C564299)
..Diabetes Mellitus, Type II, Autosomal Dominant (C562773)
..Mason-Type Diabetes (C562772)
..Maturity-Onset Diabetes of the Young, Type 1 (C565101)
..Maturity-Onset Diabetes of the Young, Type 2 (C564219)
..Maturity-Onset Diabetes of the Young, Type 3 (C563933)
..Maturity-Onset Diabetes of the Young, Type 4 (C563451)
..Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction (C565225)
..Maturity-Onset Diabetes Of The Young, Type 9 (C567393)
..MODY, Type 6 (C565231)
..Noninsulin-dependent diabetes mellitus with deafness (C536246)
..Renal cysts and diabetes syndrome (C535520)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3308
Name:	Diabetes Mellitus, Type II, Autosomal Dominant
Definition:
Alternative IDs:
ParentIDs:	MESH:D003924
TreeNumbers:	C18.452.394.750.149/C562773 \|C19.246.300/C562773
Synonyms:
Slim Mappings:	Endocrine system disease\|Metabolic disease
Reference:	MedGen: C562773 MeSH: C562773 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants