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 4th toe (HP:0010336)

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

Parent Node:
Aplasia of the phalanges of the toes (HP:0010745)

Parent Node:
Aplasia/Hypoplasia of the 4th toe (HP:0010337)

Parent Node:
Aplasia/Hypoplasia of the phalanges of the 4th toe (HP:0010371)

..Starting node
..Aplasia of the phalanges of the 4th toe (HP:0100363)

Term ID:

100363

Name:

Aplasia of the phalanges of the 4th toe

Synonym:

Absent bones of the 4th toe

Definition:

Comments:

Reference:

HP:0100363

Genes and Diseases:

Child Nodes:

........

Aplasia of the distal phalanx of the 4th toe (HP:0100379)

........

Aplasia of the middle phalanx of the 4th toe (HP:0100382)

........

Aplasia of the proximal phalanx of the 4th toe (HP:0100385)

Sister Nodes:

Aplasia/Hypoplasia of the distal phalanx of the 4th toe (HP:0100370)

Aplasia/Hypoplasia of the middle phalanx of the 4th toe (HP:0100373)

Aplasia/hypoplasia of the proximal phalanx of the 4th toe (HP:0100376)

Short phalanx of the 4th toe (HP:0100367)

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:0100363	HP:0100363	Aplasia of the phalanges of the 4th toe	0	EOGT CL E G H	285203	28526	OMIM:615297	Adams-Oliver syndrome 4	4
HP:0100363	HP:0100379	Aplasia of the distal phalanx of the 4th toe	1	CL E G H
HP:0100363	HP:0100385	Aplasia of the proximal phalanx of the 4th toe	1	CL E G H
HP:0100363	HP:0100382	Aplasia of the middle phalanx of the 4th toe	1	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.