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 ..sensory system disease ()
Child Nodes:
........auditory system disease ()
........disease of ear ()
........disease of visual system ()
........Holmes-Adie syndrome ()
........nose disease ()
........progressive external ophthalmoplegia ()
........sensory organ benign neoplasm ()
........sensory system cancer ()
........tongue 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:	5128
Name:	sensory system disease
Definition:	A disease involving the sensory system.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	disease of sensory system; disease or disorder of sensory system; disorder of sensory system; disorder of sensory system; sensory disease; sensory system disease; sensory system disease or disorder
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal