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: adenocarcinoma (MONDO:0004970)
Parent Node: in situ carcinoma (MONDO:0004647)
..Starting node ..adenocarcinoma in situ ()
Child Nodes:
........ductal breast carcinoma in situ ()
........lobular breast carcinoma in situ ()
........lung adenocarcinoma in situ ()
Sister Nodes:
..adenocarcinoma in situ ()
..bladder carcinoma in situ ()
..breast carcinoma in situ ()
..carcinoma in situ of ureter ()
..carcinoma in situ of urethra ()
..esophagus carcinoma in situ ()
..eye carcinoma in situ ()
..gall bladder carcinoma in situ ()
..intestine carcinoma in situ ()
..kidney carcinoma in situ ()
..larynx carcinoma in situ ()
..liver carcinoma in situ ()
..lung carcinoma in situ ()
..nasal cavity carcinoma in situ ()
..oral cavity carcinoma in situ ()
..pharynx carcinoma in situ ()
..prostate carcinoma in situ ()
..skin carcinoma in situ ()
..squamous carcinoma in situ ()
..stomach carcinoma in situ ()
..uterus carcinoma in situ ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	3218
Name:	adenocarcinoma in situ
Definition:	A lesion in which the normally situated glands are partially or completely replaced by atypical cells with malignant characteristics.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma in situ; AIS
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal