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 upper limb joint (HP:0009810)

Parent Node:
Abnormality of the wrist (HP:0003019)

..Starting node
..Narrow joint spaces of wrist (HP:0004048)

Term ID:

4048

Name:

Narrow joint spaces of wrist

Synonym:

Definition:

Comments:

Reference:

HP:0004048

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal carpal morphology (HP:0001191)

Decreased carpal angles of wrist (HP:0004049)

Dislocated wrist (HP:0003994)

Enlargement of the wrists (HP:0003020)

Limited wrist movement (HP:0006248)

Madelung deformity (HP:0003067)

Ulnar deviation of the wrist (HP:0003049)

Wrist flexion contracture (HP:0001239)

Wrist swelling (HP:0001225)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0004048	HP:0004048	Narrow joint spaces of wrist	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.