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 thorax morphology (HP:0000765)

Parent Node:
Abnormal clavicle morphology (HP:0000889)

..Starting node
..Medial widening of clavicles (HP:0006599)

Term ID:

6599

Name:

Medial widening of clavicles

Synonym:

Definition:

Comments:

Reference:

HP:0006599

Genes and Diseases:

Child Nodes:

Sister Nodes:

Aplasia/Hypoplasia of the clavicles (HP:0006710)

Broad clavicles (HP:0000916)

Clavicular sclerosis (HP:0100923)

Lateral clavicle hook (HP:0000895)

Long clavicles (HP:0000890)

Progressive clavicular acroosteolysis (HP:0000905)

Straight clavicles (HP:0006587)

Thin clavicles (HP:0006645)

Undulate clavicles (HP:0010560)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006599	HP:0006599	Medial widening of clavicles	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.