Disease browser and phenotype portal

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MSeqDR-LSDB
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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

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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes

Disease Browser
Parent Node: Down Syndrome (D004314)
Parent Node: Leukemoid Reaction (D007955)
..Starting node ..Myeloproliferative Syndrome, Transient (C563551)
Child Nodes:
Sister Nodes:
..Myeloproliferative Syndrome, Transient (C563551)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

7626

Name:

Myeloproliferative Syndrome, Transient

Definition:

Alternative IDs:

OMIM:159595

ParentIDs:

MESH:D004314|MESH:D007955

TreeNumbers:

C10.597.606.643.220/C563551 |C15.378.190.636.484/C563551 |C15.378.553.475.428/C563551 |C16.131.077.327/C563551 |C16.131.260.260/C563551 |C16.320.180.260/C563551

Synonyms:

Leukemia, Transient |MST |TAM |Transient Abnormal Myelopoiesis

Slim Mappings:

Blood disease|Congenital abnormality|Genetic disease (inborn)|Nervous system disease

Reference:

MedGen: C563551
MeSH: C563551
OMIM: 159595;

Genes:

Phenotypes

1	HP:0001974	Leukocytosis
2	HP:0005534	Transient myeloproliferative syndrome

Disease Causing ClinVar Variants