Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal upper limb metaphysis morphology (HP:0009809)

Parent Node:
Abnormal humeral metaphysis morphology (HP:0003907)

Parent Node:
Lytic defects in metaphyses of the upper limbs (HP:0003851)

..Starting node
..Lytic defects of the humeral metaphysis (HP:0003915)

Term ID:

3915

Name:

Lytic defects of the humeral metaphysis

Synonym:

Definition:

Comments:

Reference:

HP:0003915

Genes and Diseases:

Child Nodes:

Sister Nodes:

Lytic defects of radial metaphysis (HP:0004021)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0003915	HP:0003915	Lytic defects of the humeral metaphysis	0	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.