Human Phenotype Ontology

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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:
Anomaly of the upper limb diaphyses (HP:0009808)

Grandparent Node:
Diaphyseal sclerosis (HP:0003034)

Parent Node:
Abnormal humeral diaphysis morphology (HP:0003926)

Parent Node:
Diaphyseal sclerosis of the upper limbs (HP:0003860)

..Starting node
..Sclerosis of humeral diaphysis (HP:0003933)

Term ID:

3933

Name:

Sclerosis of humeral diaphysis

Synonym:

Increased bone density in shaft of long bone in upper arm

Definition:

Comments:

Reference:

HP:0003933

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0003933	HP:0003933	Sclerosis of humeral diaphysis	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.