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Phenotypic Abnormality (PA): Dandy-Walker malformation

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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)
+ + + + + + + 7:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + + + 6:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + + 6:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + + 5:   Abnormal axial skeleton morphology [HP:0009121] <6>(47|61) (51|30|26)
+ + + + + 5:   Abnormality of hindbrain morphology [HP:0011282] <2>(5|5) (7|2|1)
+ + + + + 5:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + + 5:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + + + 4:   Abnormality of brain morphology [HP:0012443] <13>(43|63) (53|34|15)
+ + + + 4:   Abnormality of the metencephalon [HP:0011283] <3>(5|5) (7|2|1)
+ + + + 4:   Morphological abnormality of the central nervous system [HP:0002011] <17>(60|85) (69|44|16)
+ + + + 4:   Abnormal skull morphology [HP:0000929] <14>(25|38) (28|22|20)
+ + + 3:   Abnormal cerebellum morphology [HP:0001317] <15>(5|5) (7|2|1)
+ + + 3:   Abnormality of the cerebellar vermis [HP:0002334] <6>(3|2) (4|1|0)
+ + + 3:   Central nervous system cyst [HP:0030724] <3>(2|1) (2|0|0)
+ + + 3:   Abnormality of the cerebral ventricles [HP:0002118] <11>(3|6) (6|1|3)
+ + + 3:   Abnormality of the skull base [HP:0002693] <5>(1|1) (2|0|0)
+ + 2:   Abnormality of the posterior cranial fossa [HP:0000932] <8>(1|1) (2|0|0)
+ + 2:   Abnormality of the fourth ventricle [HP:0010950] <1>(1|1) (1|0|0)
+ + 2:   Cerebellar malformation [HP:0002438] <4>(4|2) (5|1|1)
+ + 2:   Aplasia/Hypoplasia of the cerebellar vermis [HP:0006817] <4>(3|2) (4|1|0)
+ + 2:   Intracranial cystic lesion [HP:0010576] <8>(2|1) (2|0|0)
+ + 2:   Ventriculomegaly [HP:0002119] <8>(2|2) (2|0|1)
+ 1:   Widened posterior fossa [HP:0005445] <1>(1|1) (2|0|0)
+ 1:   Cerebellar cyst [HP:0002350] <2>(2|1) (2|0|0)
+ 1:   Cerebellar vermis hypoplasia [HP:0001320] <2>(2|1) (2|1|0)
+ 1:   Dilated fourth ventricle [HP:0002198] <1>(1|1) (1|0|0)
0:   Dandy-Walker malformation [HP:0001305](1|1) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
ARID-like0.00008722Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
ARID domain0.0000311Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
ARID-like0.00004003Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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