Human Phenotype Ontology 
Grandparent Node:
expandAbnormal long bone morphology (HP:0011314)help
Grandparent Node:
expandAbnormality of limb bone morphology (HP:0002813)help
Parent Node:
expandAbnormal metaphysis morphology (HP:0000944)help
..Starting node
..expandAbnormal metaphyseal vascular invasion (HP:0003562)help
Term ID: 3562
Name: Abnormal metaphyseal vascular invasion
Synonym:
Definition:
Comments:
Reference: HP:0003562
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal lower-limb metaphysis morphology (HP:0006490) help
..expandAbnormal metaphyseal trabeculation (HP:0005089) help
..expandAbnormal upper limb metaphysis morphology (HP:0009809) help
..expandAlternating radiolucent and radiodense metaphyseal lines (HP:0031016) help
..expandCorner fracture of metaphysis (HP:0003908) help
..expandDense metaphyseal bands (HP:0100959) help
..expandDumbbell-shaped metaphyses (HP:0002810) help
..expandEnlarged metaphyses (HP:0003051) help
..expandMetaphyseal cupping (HP:0003021) help
..expandMetaphyseal dysplasia (HP:0100255) help
..expandMetaphyseal enchondromatosis (HP:0005868) help
..expandMetaphyseal irregularity (HP:0003025) help
..expandMetaphyseal rarefaction (HP:0004980) help
..expandMetaphyseal sclerosis (HP:0004979) help
..expandMetaphyseal spurs (HP:0005054) help
..expandMetaphyseal striations (HP:0031367) help
..expandMetaphyseal widening (HP:0003016) help
..expandobsolete Metaphyseal dysostosis (HP:0005899) 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:0003562HP:0003562Abnormal metaphyseal vascular invasion0TRPV4 CL E G H5934118083OMIM:156530Metatropic dysplasia.214


Genes (1) :TRPV4

Diseases (1) :OMIM:156530
 

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