Human Phenotype Ontology 
Grandparent Node:
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Abnormality of finger (HP:0001167)help
Grandparent Node:
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Aplasia/hypoplasia involving bones of the hand (HP:0005927)help
Parent Node:
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Abnormal 4th finger morphology (HP:0004188)help
Parent Node:
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Aplasia/Hypoplasia of fingers (HP:0006265)help
..Starting node
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Aplasia/Hypoplasia of the 4th finger (HP:0009272)help
Term ID: 9272
Name: Aplasia/Hypoplasia of the 4th finger
Synonym: Absent/small ring finger bone; Absent/underdeveloped ring finger bone
Definition: A small/hypoplastic or absent/aplastic 4th (ring) finger.
Comments:
Reference: HP:0009272
Genes and Diseases:
 
       Child Nodes:
........expandShort 4th finger (HP:0009280) help
................... HP:0009290 Short distal phalanx of the 4th finger
................... HP:0009295 Short middle phalanx of the 4th finger
................... HP:0009301 Short proximal phalanx of the 4th finger
........expandAplasia of the 4th finger (HP:0009281) help
................... HP:0009291 Aplasia of the distal phalanx of the 4th finger
................... HP:0009294 Absent middle phalanx of 4th finger
................... HP:0009298 Aplasia of the proximal phalanx of the 4th finger

 Sister Nodes: 
..expandAplasia of the fingers (HP:0009380) help
..expandAplasia/Hypoplasia of the 2nd finger (HP:0006264) help
..expandAplasia/Hypoplasia of the 3rd finger (HP:0009318) help
..expandAplasia/Hypoplasia of the 5th finger (HP:0006262) help
..expandAplasia/Hypoplasia of the thumb (HP:0009601) help
..expandProportionate shortening of all digits (HP:0006165) help
..expandShort finger (HP:0009381) help
..expandSmall finger (HP:0030033) 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:0009272HP:0009272Aplasia/Hypoplasia of the 4th finger0 CL E G H
HP:0009272HP:0009272Aplasia/Hypoplasia of the 4th finger1 CL E G H
HP:0009272HP:0009272Aplasia/Hypoplasia of the 4th finger2 CL E G H


Genes (2) :COL2A1 GDF5

Diseases (2) :271700 615072
 

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