Human Phenotype Ontology 
Grandparent Node:
expandAbnormal upper limb bone morphology (HP:0040070)help
Grandparent Node:
expandAbnormality of the hand (HP:0001155)help
Parent Node:
expandAbnormal periosteum morphology (HP:0030313)help
Parent Node:
expandAbnormality of the metacarpal bones (HP:0001163)help
..Starting node
..expandMetacarpal periosteal thickening (HP:0006051)help
Term ID: 6051
Name: Metacarpal periosteal thickening
Synonym:
Definition:
Comments:
Reference: HP:0006051
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal 1st metacarpal morphology (HP:0010009) help
..expandAbnormal 2nd metacarpal morphology (HP:0010010) help
..expandAbnormal 3rd metacarpal morphology (HP:0010011) help
..expandAbnormal 4th metacarpal morphology (HP:0010012) help
..expandAbnormal 5th metacarpal morphology (HP:0010013) help
..expandAbnormal metacarpal epiphysis morphology (HP:0005913) help
..expandAbnormal metacarpal morphology (HP:0005916) help
..expandAbnormal metacarpophalangeal joint morphology (HP:0011911) help
..expandMetacarpal osteolysis (HP:0001504) help
..expandSupernumerary metacarpal bones (HP:0005917) 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:0006051HP:0006051Metacarpal periosteal thickening0KL CL E G H93656344OMIM:617994TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 3; HFTC368


Genes (1) :KL

Diseases (1) :OMIM:617994
 

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