MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

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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

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: disease by anatomical system (MONDO:0021199)
..Starting node ..digestive system disease ()
Child Nodes:
........angiodysplasia ()
........autoimmune disease of gastrointestinal tract ()
........Cronkhite-Canada syndrome ()
........diarrheal disease ()
........DiGeorge syndrome ()
........digestive system infectious disease ()
........digestive system neoplasm ()
........disease of pharynx ()
........gastroesophageal disease ()
........gastrointestinal allergy ()
........gastrointestinal mucositis ()
........hepatobiliary disease ()
........intestinal disease ()
........mouth disease ()
........pancreas disease ()
........peptic ulcer disease ()
........peritonitis ()
........splenic disease ()
........stomach disease ()
........upper digestive tract disease ()
Sister Nodes:
..cardiovascular disease ()
..digestive system disease ()
..disease of genitourinary system ()
..endocrine system disease ()
..hematologic disease ()
..immune system disease ()
..integumentary system disease ()
..mediastinal disease ()
..musculoskeletal system disease ()
..nervous system disorder ()
..respiratory system disease ()
..sensory system disease ()
..urinary system disease ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	4335
Name:	digestive system disease
Definition:	A disease or disorder that involves the digestive system.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	alimentary system disease; digestive disease; digestive system disease; digestive system disease or disorder; digestive system disorder; disease of digestive system; disease or disorder of digestive system; disorder of digestive system; disorder of digestive system; gastroenterological system diseas
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: SRCAP;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal