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Phenotypic Abnormality (PA): Myelodysplasia

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + 3:   Neoplasm [HP:0002664] <2>(20|21) (23|8|3)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Neoplasm by anatomical site [HP:0011793] <24>(18|19) (20|7|2)
+ + 2:   Abnormality of blood and blood-forming tissues [HP:0001871] <11>(24|35) (31|16|5)
+ 1:   Hematological neoplasm [HP:0004377] <7>(2|2) (2|1|0)
0:   Myelodysplasia [HP:0002863] <3>(0|1) (0|0|0)
- 1:   Single lineage myelodysplasia [HP:0012150] <1>(0|0) (0|0|0)
- 1:   Bilineage myelodysplasia [HP:0012149](0|0) (0|0|0)
- 1:   Multiple lineage myelodysplasia [HP:0012148](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)
RecA protein-like (ATPase-domain)0.0001427Direct


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