Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal 2nd finger morphology (HP:0004100)help
Grandparent Node:
expand
Aplasia/Hypoplasia of fingers (HP:0006265)help
Parent Node:
expand
Aplasia of the fingers (HP:0009380)help
Parent Node:
expand
Aplasia/Hypoplasia of the 2nd finger (HP:0006264)help
..Starting node
..expand
Aplasia of the 2nd finger (HP:0009535)help
Term ID: 9535
Name: Aplasia of the 2nd finger
Synonym: Absent index finger; Absent index finger phalanges; Aplasia of the index finger
Definition: Absent 2nd (index) finger.
Comments:
Reference: HP:0009535
Genes and Diseases:
 
       Child Nodes:
........expandAplasia of the distal phalanx of the 2nd finger (HP:0009565) help
........expandAbsent middle phalanx of 2nd finger (HP:0009576) help
........expandAplasia of the proximal phalanx of the 2nd finger (HP:0009596) help

 Sister Nodes: 
..expandShort 2nd finger (HP:0009536) 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:0009535HP:0009535Aplasia of the 2nd finger0 CL E G H
HP:0009535HP:0009535Aplasia of the 2nd finger1 CL E G H


Genes (0) :

Diseases (0) :
 

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