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Phenotypic Abnormality (PA): Corpus callosum atrophy

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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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + 4:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + + 3:   Morphological abnormality of the central nervous system [HP:0002011] <17>(60|85) (69|44|16)
+ + + 3:   Abnormality of the cerebral subcortex [HP:0010993] <3>(6|9) (6|2|0)
+ + + 3:   Atrophy/Degeneration affecting the central nervous system [HP:0007367] <10>(3|5) (5|3|0)
+ + + 3:   Abnormality of forebrain morphology [HP:0100547] <6>(26|32) (30|18|5)
+ + + 3:   Abnormality of brain morphology [HP:0012443] <13>(43|63) (53|34|15)
+ + 2:   Brain atrophy [HP:0012444] <3>(1|3) (3|2|0)
+ + 2:   Abnormality of the cerebral white matter [HP:0002500] <15>(6|7) (6|2|0)
+ + 2:   Aplasia/Hypoplasia involving the central nervous system [HP:0002977] <13>(19|26) (23|13|3)
+ + 2:   Abnormality of the cerebrum [HP:0002060] <16>(25|31) (29|18|5)
+ 1:   Abnormal corpus callosum morphology [HP:0001273] <7>(5|7) (5|2|0)
+ 1:   Atrophy/Degeneration affecting the cerebrum [HP:0007369] <5>(1|3) (3|2|0)
+ 1:   Cerebral white matter atrophy [HP:0012762] <1>(0|0) (0|0|0)
0:   Corpus callosum atrophy [HP:0007371](0|0) (0|0|0)