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: sheep disease (MONDO:0024985)
..Starting node ..pulmonary adenomatosis, ovine ()
Child Nodes:
Sister Nodes:
..bluetongue ()
..Nairobi sheep disease ()
..pneumonia, progressive interstitial, of sheep ()
..pulmonary adenomatosis, ovine ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	25457
Name:	pulmonary adenomatosis, ovine
Definition:	A contagious, neoplastic, pulmonary disease of sheep characterized by hyperplasia and hypertrophy of pneumocytes and epithelial cells of the lung. It is caused by jaagsiekte sheep retrovirus.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	Adenomatoses, Ovine pulmonary; Adenomatoses, pulmonary Ovine; adenomatosis, Ovine pulmonary; adenomatosis, pulmonary Ovine; adenomatosis, pulmonary, Ovine; carcinoma, Ovine pulmonary; carcinomas, Ovine pulmonary; Jaagsiekte; Ovine Adenomatoses, pulmonary; Ovine adenomatosis, pulmonary; Ovine pulmona
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal