Human Phenotype Ontology 
Grandparent Node:
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Abnormal finger phalanx morphology (HP:0005918)help
Parent Node:
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Abnormal periosteum morphology (HP:0030313)help
Parent Node:
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Abnormal proximal phalanx morphology of the hand (HP:0009834)help
..Starting node
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Proximal phalangeal periosteal thickening (HP:0006175)help
Term ID: 6175
Name: Proximal phalangeal periosteal thickening
Synonym: Thickening of connective tissue of innermost finger bone
Definition:
Comments:
Reference: HP:0006175
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
..expandSclerosis of proximal finger phalanx (HP:0100917) help
..expandSlender proximal phalanx of finger (HP:0012297) 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:0006175HP:0006175Proximal phalangeal periosteal thickening0 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 December 15 2022 release.