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: mouth disease (MONDO:0006858)
Parent Node: skeletal system disease (MONDO:0005172)
..Starting node ..tooth disease ()
Child Nodes:
........dental abscess ()
........dental fluorosis ()
........dental pulp disease ()
........inherited odontologic disease ()
........odontogenic neoplasm ()
........periodontal disease ()
........tooth erosion, non-bacterial ()
........tooth hard tissue disease ()
Sister Nodes:
..arthropathy ()
..bone disease ()
..bone marrow disease ()
..cartilage disease ()
..flatfoot ()
..mixed connective tissue disease ()
..necrosis of ear ossicle ()
..ossification of the posterior longitudinal ligament of the spine ()
..patellar tendinitis ()
..rare odontologic disease ()
..rheumatic fever ()
..skeletal ligament disease ()
..skeletal tuberculosis ()
..sternal neoplasm ()
..symphalangism ()
..tooth disease ()
..vertebral column disease ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	6999
Name:	tooth disease
Definition:	A disease involving the calcareous tooth.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	calcareous tooth disease; calcareous tooth disease or disorder; dental disorder; disease of calcareous tooth; disease or disorder of calcareous tooth; disorder of calcareous tooth; disorder of calcareous tooth; tooth disorder
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal