Human Phenotype Ontology 
Grandparent Node:
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Abnormal finger phalanx morphology (HP:0005918)help
Parent Node:
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Abnormal proximal phalanx morphology of the hand (HP:0009834)help
..Starting node
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Slender proximal phalanx of finger (HP:0012297)help
Term ID: 12297
Name: Slender proximal phalanx of finger
Synonym: Slender innermost bone of finger
Definition: Reduced diameter of the proximal phalanx of finger.
Comments:
Reference: HP:0012297
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of the epiphyses of the proximal phalanges of the hand (HP:0010245) help
..expandAplasia/Hypoplasia of the proximal phalanges of the hand (HP:0009851) help
..expandBroad proximal phalanges of the hand (HP:0009852) help
..expandBullet-shaped proximal phalanges of the hand (HP:0009853) help
..expandCurved proximal phalanges of the hand (HP:0009854) help
..expandDuplication of the middle phalanx of hand (HP:0010008) help
..expandLong proximal phalanx of finger (HP:0006127) help
..expandOsteolytic defects of the proximal phalanges of the hand (HP:0009855) help
..expandProximal phalangeal periosteal thickening (HP:0006175) help
..expandSclerosis of proximal finger phalanx (HP:0100917) help
..expandSymphalangism affecting the proximal phalanges of the hand (HP:0009857) help
..expandThin proximal phalanges with broad epiphyses of the hand (HP:0006213) help
..expandTombstone-shaped proximal phalanges (HP:0006060) help
..expandTriangular shaped proximal phalanges of the hand (HP:0009858) 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:0012297HP:0012297Slender proximal phalanx of finger0KIF22 CL E G H38356391OMIM:603546Spondyloepimetaphyseal dysplasia with joint laxity, type 2.14


Genes (1) :KIF22

Diseases (1) :OMIM:603546
 

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