Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of finger (HP:0001167)help
Grandparent Node:
expandAplasia/hypoplasia involving bones of the hand (HP:0005927)help
Parent Node:
expandAplasia/Hypoplasia of fingers (HP:0006265)help
..Starting node
..expandSmall finger (HP:0030033)help
Term ID: 30033
Name: Small finger
Synonym: Small finger
Definition: Significant reduction in both length and girth of the finger compared to the contralateral finger, or alternatively, compared to a typical finger size for an age-matched individual.
Comments:
Reference: HP:0030033
Genes and Diseases:
 
       Child Nodes:

 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 4th finger (HP:0009272) 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
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030033HP:0030033Small finger0IHH CL E G H35495956OMIM:607778Acrocapitofemoral dysplasia.44
HP:0030033HP:0030033Small finger0KCNJ2 CL E G H37596263OMIM:170390Andersen cardiodysrhythmic periodic paralysis193


Genes (2) :IHH KCNJ2

Diseases (2) :OMIM:607778 OMIM:170390
 

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