Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the middle phalanx of the 5th finger (HP:0004219)help
Grandparent Node:
expandAplasia/Hypoplasia of the phalanges of the 5th finger (HP:0009376)help
Parent Node:
expandAplasia of the 5th finger (HP:0009238)help
Parent Node:
expandAplasia of the middle phalanx of the hand (HP:0010239)help
Parent Node:
expandAplasia/Hypoplasia of the middle phalanx of the 5th finger (HP:0009161)help
..Starting node
..expandAbsent middle phalanx of 5th finger (HP:0009162)help
Term ID: 9162
Name: Absent middle phalanx of 5th finger
Synonym: Absent middle bone of little finger; Absent middle bone of pinkie finger; Absent middle bone of pinky finger; Aplasia of the middle phalanx of the 5th finger
Definition: Absence of the middle phalanx of the little (5th) finger.
Comments:
Reference: HP:0009162
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandShort middle phalanx of the 5th finger (HP:0004220) 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:0009162HP:0009162Absent middle phalanx of 5th finger0ATP6V1B2 CL E G H526854OMIM:124480Deafness, congenital, and onychodystrophy, autosomal dominant5
HP:0009162HP:0009162Absent middle phalanx of 5th finger0GJA1 CL E G H26974274OMIM:186100Syndactyly, type III.68
HP:0009162HP:0009162Absent middle phalanx of 5th finger0IFT140 CL E G H974229077OMIM:266920Short-rib thoracic dysplasia 9 with or without polydactyly148


Genes (3) :ATP6V1B2 GJA1 IFT140

Diseases (3) :OMIM:124480 OMIM:186100 OMIM:266920
 

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