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 distal phalanx of the 3rd toe (HP:0010368)

Grandparent Node:
Aplasia/Hypoplasia of the 3rd toe (HP:0010331)

Grandparent Node:
Aplasia/Hypoplasia of the distal phalanges of the toes (HP:0010185)

Grandparent Node:
Aplasia/Hypoplasia of the phalanges of the 3rd toe (HP:0010359)

Parent Node:
Aplasia of the distal phalanges of the toes (HP:0010645)

Parent Node:
Aplasia of the phalanges of the 3rd toe (HP:0100362)

Parent Node:
Aplasia/Hypoplasia of the distal phalanx of the 3rd toe (HP:0100369)

..Starting node
..Absent distal phalanx of the 3rd toe (HP:0100378)

Term ID:

100378

Name:

Absent distal phalanx of the 3rd toe

Synonym:

Absent distal phalanx of the third toe; Absent outermost bone of the 3rd toe; Aplasia of the distal phalanx of the 3rd toe

Definition:

Developmental aplasia of the distal phalanx of third toe.

Comments:

Reference:

HP:0100378

Genes and Diseases:

Child Nodes:

Sister Nodes:

Short distal phalanx of the 3rd toe (HP:0100389)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100378	HP:0100378	Absent distal 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.