Disease browser and phenotype 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

Disease Browser
Parent Node: Cat Diseases (D002371)
Parent Node: Leukemia (D007938)
Parent Node: Retroviridae Infections (D012192)
..Starting node ..Leukemia, Feline (D016582)
Child Nodes:
Sister Nodes:
..Avian Leukosis (D001353)
..Deltaretrovirus Infections (D006800) 4
..Human spumaretrovirus infection (C536069)
..Lentivirus Infections (D016180) 18
..Leukemia, Feline (D016582)
..Murine Acquired Immunodeficiency Syndrome (D016183)
..Pulmonary Adenomatosis, Ovine (D011648)
..Sarcoma, Avian (D001357)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6339
Name:	Leukemia, Feline
Definition:	A neoplastic disease of cats frequently associated with feline leukemia virus infection.
Alternative IDs:
ParentIDs:	MESH:D002371\|MESH:D007938\|MESH:D012192
TreeNumbers:	C02.782.815.622 \|C04.557.337.385 \|C22.180.500
Synonyms:	Feline Leukemia \|Feline Leukemias \|Leukemias, Feline
Slim Mappings:	Animal disease\|Cancer\|Viral disease
Reference:	MedGen: D016582 MeSH: D016582 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants