Human Phenotype Ontology 
Grandparent Node:
expandAbnormal femoral head morphology (HP:0003368)help
Grandparent Node:
expandAbnormality of femoral epiphysis (HP:0006499)help
Parent Node:
expandAbnormal ossification involving the femoral head and neck (HP:0009107)help
Parent Node:
expandAbnormality of the epiphysis of the femoral head (HP:0010574)help
..Starting node
..expandMulticentric ossification of proximal femoral epiphyses (HP:0006450)help
Term ID: 6450
Name: Multicentric ossification of proximal femoral epiphyses
Synonym:
Definition:
Comments:
Reference: HP:0006450
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAplasia/Hypoplasia of the capital femoral epiphysis (HP:0005003) help
..expandAvascular necrosis of the capital femoral epiphysis (HP:0005743) help
..expandCone-shaped capital femoral epiphysis (HP:0008789) help
..expandDelayed proximal femoral epiphyseal ossification (HP:0008828) help
..expandEarly ossification of capital femoral epiphyses (HP:0008797) help
..expandEnlargement of the proximal femoral epiphysis (HP:0003371) help
..expandFlat capital femoral epiphysis (HP:0003370) help
..expandIrregular capital femoral epiphysis (HP:0005041) help
..expandProximal femoral epiphysiolysis (HP:0006461) help
..expandWide capital femoral epiphyses (HP:0008784) 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:0006450HP:0006450Multicentric ossification of proximal femoral epiphyses0DYM CL E G H5480821317OMIM:223800Dyggve-Melchior-Clausen disease.65


Genes (1) :DYM

Diseases (1) :OMIM:223800
 

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