Human Phenotype Ontology 
Grandparent Node:
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Anonychia (HP:0001798)help
Grandparent Node:
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Aplastic/hypoplastic toenail (HP:0010624)help
Parent Node:
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Absent toenail (HP:0001802)help
..Starting node
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Absent fifth toenail (HP:0200105)help
Term ID: 200105
Name: Absent fifth toenail
Synonym: Absent fifth toenail; Missing fifth toenail
Definition:
Comments:
Reference: HP:0200105
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbsent nail of hallux (HP:0012555) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0200105HP:0200105Absent fifth toenail0ARID1A CL E G H828911110OMIM:614607Coffin-Siris syndrome 288
HP:0200105HP:0200105Absent fifth toenail0PIGF CL E G H52818962OMIM:619356ONYCHODYSTROPHY, OSTEODYSTROPHY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES SYNDROME; OORS


Genes (2) :ARID1A PIGF

Diseases (2) :OMIM:614607 OMIM:619356
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.