Human Phenotype Ontology 
Grandparent Node:
expandAplasia/Hypoplasia of fingers (HP:0006265)help
Parent Node:
expandAbsent toe (HP:0010760)help
Parent Node:
expandAplasia of the fingers (HP:0009380)help
..Starting node
..expandAdactyly (HP:0009776)help
Term ID: 9776
Name: Adactyly
Synonym: Absent fingers or toes; Aphalangy
Definition: The absence of all phalanges of all the digits of a limb and the associated soft tissues.
Comments:
Reference: HP:0009776
Genes and Diseases:
 
       Child Nodes:
........expandAphalangy of hands and feet (HP:0200113) help

 Sister Nodes: 
..expandAbsent thumb (HP:0009777) help
..expandAplasia of the 2nd finger (HP:0009535) help
..expandAplasia of the 3rd finger (HP:0009460) help
..expandAplasia of the 4th finger (HP:0009281) help
..expandAplasia of the 5th finger (HP:0009238) help
..expandAplasia of the distal phalanges of the hand (HP:0009881) help
..expandAplasia of the middle phalanx of the hand (HP:0010239) help
..expandAplasia of the proximal phalanges of the hand (HP:0010242) help
..expandHand oligodactyly (HP:0001180) 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:0009776HP:0009776Adactyly0NEK1 CL E G H47507744ORPHA:2751Orofaciodigital syndrome type 2HP:0040284 - Very rare101
HP:0009776HP:0200113Aphalangy of hands and feet1 CL E G H


Genes (1) :NEK1

Diseases (1) :ORPHA:2751
 

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