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 foot morphology (HP:0001760)

Grandparent Node:
Osteolysis involving bones of the lower limbs (HP:0009139)

Parent Node:
Abnormal talus morphology (HP:0008365)

Parent Node:
Osteolysis involving bones of the feet (HP:0009134)

..Starting node
..Osteolysis of talus (HP:0008095)

Term ID:

8095

Name:

Osteolysis of talus

Synonym:

Osteolysis of tali

Definition:

Osteolysis affecting the talus.

Comments:

Reference:

HP:0008095

Genes and Diseases:

Child Nodes:

Sister Nodes:

Metatarsal osteolysis (HP:0001473)

Osteolysis involving tarsal bones (HP:0006234)

Osteolytic defects of the phalanges of the toes (HP:0010177)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008095	HP:0008095	Osteolysis of talus	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.