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Phenotypic Abnormality (PA): Anencephaly

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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>(147|170) (164|102|45)
+ + + + 4:   Abnormality of nervous system morphology [HP:0012639] <5>(70|97) (81|48|16)
+ + + + 4:   Abnormality of brain morphology [HP:0012443] <13>(44|63) (54|31|14)
+ + + 3:   Abnormality of forebrain morphology [HP:0100547] <6>(26|28) (29|15|4)
+ + + 3:   Morphological abnormality of the central nervous system [HP:0002011] <17>(61|85) (71|41|16)
+ + 2:   Abnormality of the cerebrum [HP:0002060] <16>(25|27) (28|15|4)
+ + 2:   Aplasia/Hypoplasia involving the central nervous system [HP:0002977] <13>(18|22) (22|10|2)
+ 1:   Aplasia/Hypoplasia of the cerebrum [HP:0007364] <5>(11|15) (12|5|1)
0:   Anencephaly [HP:0002323] <2>(0|1) (0|0|0)
- 1:   Arrhinencephaly [HP:0002139](0|0) (0|0|0)
- 1:   Hydranencephaly [HP:0002324](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)
T-box0.0001853Direct


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