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Phenotypic Abnormality (PA): Alopecia of scalp

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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)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + 4:   Abnormality of the integument [HP:0001574] <4>(48|69) (59|36|15)
+ + + 3:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + 3:   Abnormality of skin adnexa morphology [HP:0011138] <5>(16|19) (17|6|2)
+ + 2:   Abnormal hair morphology [HP:0001595] <12>(14|18) (15|4|1)
+ + 2:   Abnormality of the scalp [HP:0001965] <4>(4|4) (4|1|0)
+ + 2:   Abnormal hair quantity [HP:0011362] <8>(5|8) (6|3|0)
+ 1:   Alopecia [HP:0001596] <6>(1|4) (1|2|0)
+ 1:   Abnormality of the scalp hair [HP:0100037] <5>(4|4) (4|1|0)
0:   Alopecia of scalp [HP:0002293] <1>(0|1) (0|1|0)
- 1:   Scarring alopecia of scalp [HP:0004552](0|1) (0|1|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Laminin-type module0.0002041Direct


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Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.002543Inherited