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: integumentary system disease (MONDO:0002051)
Parent Node: mouth disease (MONDO:0006858)
..Starting node ..lip disease ()
Child Nodes:
........cheilitis ()
........herpes labialis ()
........lip neoplasm ()
........lower lip fistula ()
Sister Nodes:
..adenoid hypertrophy ()
..alveolar periostitis ()
..burning mouth syndrome ()
..commissural lip fistula ()
..lichen planus, oral ()
..lip disease ()
..Ludwig's angina ()
..maxillary sinus cholesteatoma ()
..maxillary sinusitis ()
..mouth mucosa disease ()
..neoplasm of floor of mouth ()
..neoplasm of jaw ()
..odontoma ()
..oral candidiasis ()
..oral cavity neoplasm ()
..oral Crohn disease ()
..oral hairy leukoplakia ()
..oral leukoedema ()
..oral submucous fibrosis ()
..oral tuberculosis ()
..salivary gland disease ()
..tongue disease ()
..tooth disease ()
..uvulitis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	4748
Name:	lip disease
Definition:	A disease involving the lip.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	disease of lip; disease of lips; disease or disorder of lip; disorder of lip; disorder of lip; lip disease; lip disease or disorder; lip disorder
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal