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 phalanges of the 3rd toe (HP:0010330)

Grandparent Node:
Aplasia/Hypoplasia of the phalanges of the toes (HP:0010173)

Parent Node:
Abnormal morphology of the proximal phalanx of the 3rd toe (HP:0010370)

Parent Node:
Aplasia/hypoplasia of proximal toe phalanx (HP:0010203)

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

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

..Starting node
..Aplasia/hypoplasia of the proximal phalanx of the 3rd toe (HP:0100375)

Term ID:

100375

Name:

Aplasia/hypoplasia of the proximal phalanx of the 3rd toe

Synonym:

Absent/small innermost bone of 3rd toe; Absent/underdeveloped innermost bone of 3rd toe

Definition:

Absence (agenesis) or underdevelopment of the proximal phalanx of the 3rd toe.

Comments:

Reference:

HP:0100375

Genes and Diseases:

Child Nodes:

........

Absent proximal phalanx of the 3rd toe (HP:0100384)

........

Short proximal phalanx of the 3rd toe (HP:0100395)

Sister Nodes:

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

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

Aplasia/Hypoplasia of the middle phalanx of the 3rd toe (HP:0100372)

Short phalanx of the 3rd toe (HP:0100366)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100375	HP:0100375	Aplasia/hypoplasia of the proximal phalanx of the 3rd toe	0	CL E G H
HP:0100375	HP:0100384	Absent proximal phalanx of the 3rd toe	1	CL E G H
HP:0100375	HP:0100395	Short proximal phalanx of the 3rd toe	1	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.