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:
Abnormal cortical bone morphology (HP:0003103)

Parent Node:
Abnormal morphology of the cortex of the humerus (HP:0010629)

Parent Node:
Thin bony cortex (HP:0002753)

..Starting node
..Humeral cortical thinning (HP:0003869)

Term ID:

3869

Name:

Humeral cortical thinning

Synonym:

Definition:

Comments:

Reference:

HP:0003869

Genes and Diseases:

Child Nodes:

Sister Nodes:

Cortical thinning of hand bones (HP:0004272)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0003869	HP:0003869	Humeral cortical thinning	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.