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Disease Ontology (DO): holoprosencephaly

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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)
+ + + 3:   disease [DOID:4] <8>
+ + 2:   physical disorder [DOID:0080015] <20>(5|9) (6|0|1)
+ 1:   congenital nervous system abnormality [DOID:2490] <5>(1|1) (1|0|0)
0:   holoprosencephaly [DOID:4621] <10>(0|0) (0|0|0)
- 1:   holoprosencephaly 1 [DOID:0110881](0|0) (0|0|0)
- 1:   holoprosencephaly 11 [DOID:0110877](0|0) (0|0|0)
- 1:   holoprosencephaly 2 [DOID:0110872](0|0) (0|0|0)
- 1:   holoprosencephaly 3 [DOID:0110875](0|0) (0|0|0)
- 1:   holoprosencephaly 4 [DOID:0110880](0|0) (0|0|0)
- 1:   holoprosencephaly 5 [DOID:0110878](0|0) (0|0|0)
- 1:   holoprosencephaly 6 [DOID:0110874](0|0) (0|0|0)
- 1:   holoprosencephaly 7 [DOID:0110876](0|0) (0|0|0)
- 1:   holoprosencephaly 8 [DOID:0110879](0|0) (0|0|0)
- 1:   holoprosencephaly 9 [DOID:0110873](0|0) (0|0|0)