Human Phenotype Ontology 
Grandparent Node:
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Aplasia/Hypoplasia of the middle phalanges of the hand (HP:0009843)help
Grandparent Node:
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Short finger (HP:0009381)help
Grandparent Node:
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Short phalanx of finger (HP:0009803)help
Parent Node:
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Aplasia/Hypoplasia of the middle phalanx of the 4th finger (HP:0009299)help
Parent Node:
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Short 4th finger (HP:0009280)help
Parent Node:
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Short middle phalanx of finger (HP:0005819)help
..Starting node
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Short middle phalanx of the 4th finger (HP:0009295)help
Term ID: 9295
Name: Short middle phalanx of the 4th finger
Synonym: Brachymesophalangy IV (finger); Hypoplastic/small middle phalanx of ring finger; Hypoplastic/small middle phalanx of the 4th finger; Short middle bone of 4th finger; Short middle phalanx of ring finger
Definition: Hypoplastic/small middle phalanx of the 4th finger, also known as the ring finger.
Comments:
Reference: HP:0009295
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandShort middle phalanx of the 2nd finger (HP:0009577) help
..expandShort middle phalanx of the 3rd finger (HP:0009439) help
..expandShort middle phalanx of the 5th finger (HP:0004220) help
..expandShort proximal phalanx of thumb (HP:0009638) help
..expandShortening of all middle phalanges of the fingers (HP:0006110) 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:0009295HP:0009295Short middle phalanx of the 4th finger0GDF5 CL E G H82004220OMIM:615072Brachydactyly, type A1, C52
HP:0009295HP:0009295Short middle phalanx of the 4th finger0MECOM CL E G H21223498OMIM:616738RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2; RUSAT24
HP:0009295HP:0009295Short middle phalanx of the 4th finger0NOG CL E G H92417866OMIM:186500Multiple synostoses syndrome 122


Genes (3) :GDF5 MECOM NOG

Diseases (3) :OMIM:615072 OMIM:616738 OMIM:186500
 

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