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:
Abnormality of the hand (HP:0001155)

Grandparent Node:
Osteolysis involving bones of the upper limbs (HP:0045039)

Parent Node:
Abnormality of the scaphoid (HP:0004243)

Parent Node:
Osteolytic defects of the hand bones (HP:0009699)

..Starting node
..Osteolysis of scaphoids (HP:0006202)

Term ID:

6202

Name:

Osteolysis of scaphoids

Synonym:

Definition:

Comments:

Reference:

HP:0006202

Genes and Diseases:

Child Nodes:

Sister Nodes:

Osteolytic defects of the phalanges of the hand (HP:0009771)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006202	HP:0006202	Osteolysis of scaphoids	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.