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: bone marrow cancer (MONDO:0021138)
Parent Node: hairy cell leukemia (MONDO:0018935)
Parent Node: lymph node cancer (MONDO:0001082)
Parent Node: primary bone lymphoma (MONDO:0017814)
..Starting node ..intrapelvic lymph node leukemic reticuloendotheliosis ()
Child Nodes:
Sister Nodes:
..adult T-cell leukemia/lymphoma ()
..childhood acute lymphoblastic leukemia ()
..intrapelvic lymph node leukemic reticuloendotheliosis ()
..paranasal sinus lymphoma ()
..splenic manifestation of hairy cell leukemia ()
..sternum lymphoma ()
..T-cell childhood lymphoblastic lymphoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1607
Name:	intrapelvic lymph node leukemic reticuloendotheliosis
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	leukemic reticuloendotheliosis involving intrapelvic lymph nodes; leukemic reticuloendotheliosis of intrapelvic lymph nodes
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal