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:
Abnormal epiphysis morphology (HP:0005930)

Parent Node:
Abnormality of radial epiphyses (HP:0003999)

Parent Node:
Small epiphyses (HP:0010585)

..Starting node
..Small radial epiphyses (HP:0004010)

Term ID:

4010

Name:

Small radial epiphyses

Synonym:

Definition:

Comments:

Reference:

HP:0004010

Genes and Diseases:

Child Nodes:

Sister Nodes:

Small epiphyses of the metacarpals (HP:0009194)

Small epiphyses of the phalanges of the hand (HP:0010236)

Small epiphyses of the toes (HP:0010170)

Small epiphyses of the upper limbs (HP:0003844)

Small proximal tibial epiphyses (HP:0012284)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0004010	HP:0004010	Small radial epiphyses	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.