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:
Sclerosis of 3rd toe phalanx (HP:0100927)

Grandparent Node:
Sclerosis of middle toe phalanx (HP:0100947)

Parent Node:
Patchy sclerosis of 3rd toe phalanx (HP:0010364)

Parent Node:
Patchy sclerosis of middle toe phalanx (HP:0010199)

Parent Node:
Sclerosis of the middle phalanx of the 3rd toe (HP:0100936)

..Starting node
..Patchy sclerosis of the middle phalanx of the 3rd toe (HP:0100461)

Term ID:

100461

Name:

Patchy sclerosis of the middle phalanx of the 3rd toe

Synonym:

Uneven increase in bone density in the middle bone of the 3rd toe

Definition:

Comments:

Reference:

HP:0100461

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:0100461	HP:0100461	Patchy sclerosis of the middle phalanx of the 3rd toe	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.