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Phenotypic Abnormality (PA): Congenital, generalized hypertrichosis

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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 integument [HP:0001574] <4>(48|69) (59|37|15)
+ + + + 4:   Abnormality of skin adnexa morphology [HP:0011138] <5>(16|19) (17|6|2)
+ + + 3:   Abnormal hair morphology [HP:0001595] <12>(14|18) (15|4|1)
+ + 2:   Abnormal hair quantity [HP:0011362] <8>(5|8) (6|3|0)
+ 1:   Hypertrichosis [HP:0000998] <8>(1|2) (1|0|0)
0:   Congenital, generalized hypertrichosis [HP:0004540](0|1) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
ABC transporter ATPase domain-like0.00002346Direct


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