Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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 distal phalanx of the 2nd toe (HP:0010356)

Grandparent Node:
Sclerosis of 2nd toe phalanx (HP:0100926)

Grandparent Node:
Sclerosis of distal toe phalanx (HP:0100948)

Parent Node:
Patchy sclerosis of 2nd toe phalanx (HP:0010352)

Parent Node:
Patchy sclerosis of distal toe phalanx (HP:0010190)

Parent Node:
Sclerosis of the distal phalanx of the 2nd toe (HP:0100939)

..Starting node
..Patchy sclerosis of the distal phalanx of the 2nd toe (HP:0010418)

Term ID:

10418

Name:

Patchy sclerosis of the distal phalanx of the 2nd toe

Synonym:

Uneven increase in bone density in the outermost bone of the 2nd toe

Definition:

Comments:

Reference:

HP:0010418

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:0010418	HP:0010418	Patchy sclerosis of the distal phalanx of the 2nd 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.