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Phenotypic Abnormality (PA): Clinodactyly

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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 the skeletal system [HP:0000924] <7>(89|98) (94|51|33)
+ + + + 4:   Abnormality of skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + + + 4:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + + 3:   Abnormality of limb bone [HP:0040068] <1>(28|30) (30|18|20)
+ + + 3:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|41) (38|23|23)
+ + 2:   Abnormality of limb bone morphology [HP:0002813] <13>(28|30) (30|18|20)
+ 1:   Abnormal digit morphology [HP:0011297] <10>(16|19) (17|14|16)
0:   Clinodactyly [HP:0030084] <2>(0|3) (2|0|0)
- 1:   Finger clinodactyly [HP:0040019] <5>(0|1) (0|0|0)
- 1:   Toe clinodactyly [HP:0001863] <5>(0|0) (1|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Insulin-like0.0006867Direct
ZZ domain0.0006867Direct
Erythroid transcription factor GATA-10.07519Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Insulin-like0.0006827Direct
Cysteine proteinases0.4353Inherited


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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