SUPERFAMILY 1.75 HMM library and genome assignments server

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Disease Ontology (DO): aplastic anemia

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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Root: DO Hierarchy (disease ontology from University of Maryland)

Shortest distance to current term (+ for parents, - for children) DO term [DO ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   disease [DOID:4] <8>
+ + + 3:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + 2:   hematopoietic system disease [DOID:74] <7>(27|29) (27|15|8)
+ 1:   anemia [DOID:2355] <8>(4|5) (4|2|1)
0:   aplastic anemia [DOID:12449] <4>(0|2) (0|0|0)
- 1:   sideroblastic anemia [DOID:8955] <6>(0|0) (0|0|0)
- 1:   congenital hypoplastic anemia [DOID:1342] <2>(0|0) (0|0|0)
- 1:   myelophthisic anemia [DOID:2354](0|0) (0|0|0)
- 1:   pure red-cell aplasia [DOID:1340](0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Short-chain cytokines0.00000255Direct
Erythroid transcription factor GATA-10.000006357Direct


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