Human Phenotype Ontology 
Grandparent Node:
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Aplasia/Hypoplasia of fingers (HP:0006265)help
Parent Node:
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Absent toe (HP:0010760)help
Parent Node:
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Aplasia of the fingers (HP:0009380)help
..Starting node
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Adactyly (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 entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009776HP:0009776Adactyly0DOLK CL E G H2284591131ORPHA01121523406610746
HP:0009776HP:0009776Adactyly0NEK1 CL E G H47502751Hunter Carpenter Macdonald syndromeORPHA0303117744604588
HP:0009776HP:0009776Adactyly1DOLK CL E G H2284591131ORPHA01121523406610746
HP:0009776HP:0009776Adactyly1NEK1 CL E G H47502751Hunter Carpenter Macdonald syndromeORPHA0303117744604588


Genes (2) :DOLK NEK1

Diseases (2) :91131 2751
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.