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:
Aplasia/Hypoplasia of the phalanges of the thumb (HP:0009658)

Grandparent Node:
Aplasia/Hypoplasia of the thumb (HP:0009601)

Parent Node:
Aplasia of the distal phalanges of the hand (HP:0009881)

Parent Node:
Aplasia/Hypoplasia of the distal phalanx of the thumb (HP:0009641)

Parent Node:
Partial absence of thumb (HP:0009659)

..Starting node
..Aplasia of the distal phalanx of the thumb (HP:0009649)

Term ID:

9649

Name:

Aplasia of the distal phalanx of the thumb

Synonym:

Absence of the outermost bone of the thumb; Absent ossification/absent terminal thumb phalanx; Aplasia of the outermost bone of the thumb

Definition:

Absence of the distal/terminal phalanx of the thumb.

Comments:

Reference:

HP:0009649

Genes and Diseases:

Child Nodes:

Sister Nodes:

Absent proximal phalanx of thumb (HP:0009637)

Aplasia of the 1st metacarpal (HP:0010035)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009649	HP:0009649	Aplasia of the distal phalanx of the thumb	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.