dcGO - A comprehensive domain-centric ontology resource for post-genomic research on functions, phenotypes, diseases and more   
  
  

Phenotypic Abnormality (PA): Thin skin

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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> #Domains
(Superfamily|Family)
#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 the skin [HP:0000951] <4>(34|55) (45|36|12)
+ + + 3:   Abnormality of skin morphology [HP:0011121] <22>(29|49) (40|31|11)
+ + 2:   Localized skin lesion [HP:0011355] <29>(12|20) (18|10|6)
+ 1:   Aplasia/Hypoplasia of the skin [HP:0008065] <8>(4|4) (5|2|1)
0:   Thin skin [HP:0000963](0|1) (0|0|0)