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 middle phalanx of the 3rd toe (HP:0010369)

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

Grandparent Node:
Aplasia/Hypoplasia of the middle phalanges of the toes (HP:0010194)

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

Parent Node:
Aplasia of the middle phalanges of the toes (HP:0100387)

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

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

..Starting node
..Absent middle phalanx of the 3rd toe (HP:0100381)

Term ID:

100381

Name:

Absent middle phalanx of the 3rd toe

Synonym:

Absent middle bone of the 3rd toe; Absent middle phalanx of the third toe; Aplasia of the middle phalanx of the 3rd toe

Definition:

Developmental aplasia of the middle phalanx of third toe.

Comments:

Reference:

HP:0100381

Genes and Diseases:

Child Nodes:

Sister Nodes:

Short middle phalanx of the 3rd toe (HP:0100392)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100381	HP:0100381	Absent middle phalanx of the 3rd toe	0	EOGT CL E G H	285203	28526	OMIM:615297	Adams-Oliver syndrome 4	4

Genes (1) :EOGT

Diseases (1) :OMIM:615297

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.