Human Phenotype Ontology 
Grandparent Node:
expandAbnormal metaphysis morphology (HP:0000944)help
Grandparent Node:
expandAbnormality of the upper limb (HP:0002817)help
Parent Node:
expandAbnormal upper limb metaphysis morphology (HP:0009809)help
..Starting node
..expandLytic defects in metaphyses of the upper limbs (HP:0003851)help
Term ID: 3851
Name: Lytic defects in metaphyses of the upper limbs
Synonym:
Definition:
Comments:
Reference: HP:0003851
Genes and Diseases:
 
       Child Nodes:
........expandLytic defects of the humeral metaphysis (HP:0003915) help
........expandLytic defects of radial metaphysis (HP:0004021) help

 Sister Nodes: 
..expandAbnormal elbow metaphysis morphology (HP:0003949) help
..expandAbnormal hand metaphysis morphology (HP:0005923) help
..expandAbnormal humeral metaphysis morphology (HP:0003907) help
..expandAbnormal radial metaphysis morphology (HP:0004015) help
..expandAbnormal ulnar metaphysis morphology (HP:0004039) help
..expandCupped metaphyses of the upper limbs (HP:0003848) help
..expandNormal density transverse bands in metaphyses of the upper limbs (HP:0003852) help
..expandSclerosis of metaphyses of the upper limbs (HP:0003854) help
..expandSpurred metaphyses of the upper limbs (HP:0003855) help
..expandUpper limb metaphyseal widening (HP:0003856) help
..expandUpper-limb metaphyseal irregularity (HP:0003850) 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:0003851HP:0003851Lytic defects in metaphyses of the upper limbs0 CL E G H
HP:0003851HP:0004021Lytic defects of radial metaphysis1 CL E G H
HP:0003851HP:0003915Lytic defects of the humeral metaphysis1 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.