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Phenotypic Abnormality (PA): Lethal skeletal dysplasia

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + 2:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ 1:   Skeletal dysplasia [HP:0002652] <9>(1|0) (2|0|0)
0:   Lethal skeletal dysplasia [HP:0005716](0|0) (1|0|0)

Supra-domain (Single|Duplex|Triple)

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Supra-domain (Single)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
WD40 repeat-like0.0005631Direct

LINKTO: Supra-domain2BO Download and Supra-domain2BO Algorithm

Distribution on sTOL

Plot distribution on species Tree Of Life (sTOL) for single supra-domains annotated by this HP term
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