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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: Down Syndrome (D004314)
Parent Node: Myeloproliferative Disorders (D009196)
..Starting node ..Transient Myeloproliferative Disorder of Down Syndrome (C566024)
Child Nodes:
Sister Nodes:
..Anemia, Myelophthisic (D000750)
..Leukemia, Erythroblastic, Acute (D004915) 1
..Leukemia, Myelogenous, Chronic, BCR-ABL Positive (D015464) 3
..Leukemia, Neutrophilic, Chronic (D015467)
..Leukemoid Reaction (D007955) 1
..Myeloproliferative Disease, Autosomal Recessive (C564977)
..Myeloproliferative Disorder, Chronic, with Eosinophilia (C565054)
..Polycythemia Vera (D011087) 2
..Primary Myelofibrosis (D055728) 2
..Thrombocytosis (D013922) 4
..Transient Myeloproliferative Disorder of Down Syndrome (C566024)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11202
Name:	Transient Myeloproliferative Disorder of Down Syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D004314\|MESH:D009196
TreeNumbers:	C10.597.606.643.220/C566024 \|C15.378.190.636/C566024 \|C16.131.077.327/C566024 \|C16.131.260.260/C566024 \|C16.320.180.260/C566024
Synonyms:
Slim Mappings:	Blood disease\|Congenital abnormality\|Genetic disease (inborn)\|Nervous system disease
Reference:	MedGen: C566024 MeSH: C566024 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants