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Phenotypic Abnormality (PA): Agenesis of pineal gland

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + 3:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + + 3:   Abnormality of the endocrine system [HP:0000818] <16>(28|35) (35|13|5)
+ + 2:   Abnormality of brain morphology [HP:0012443] <13>(43|63) (53|34|15)
+ + 2:   Morphological abnormality of the central nervous system [HP:0002011] <17>(60|85) (69|44|16)
+ + 2:   Abnormality of the pineal gland [HP:0012680] <2>(0|0) (0|0|0)
+ 1:   Aplasia/Hypoplasia involving the central nervous system [HP:0002977] <13>(19|26) (23|13|3)
+ 1:   Abnormality of pineal morphology [HP:0012681] <4>(0|0) (0|0|0)
0:   Agenesis of pineal gland [HP:0012687](0|0) (0|0|0)