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 4th finger morphology (HP:0004188)

Grandparent Node:
Flexion contracture of finger (HP:0012785)

Parent Node:
Joint contracture of the 4th finger (HP:0009274)

..Starting node
..Contracture of the metacarpophalangeal joint of the 4th finger (HP:0009277)

Term ID:

9277

Name:

Contracture of the metacarpophalangeal joint of the 4th finger

Synonym:

Definition:

Chronic loss of joint motion of the metacarpophalangeal joint of the 4th finger due to structural changes in non-bony tissue.

Comments:

Reference:

HP:0009277

Genes and Diseases:

Child Nodes:

Sister Nodes:

Contracture of the distal interphalangeal joint of the 4th finger (HP:0009275)

Contracture of the proximal interphalangeal joint of the 4th finger (HP:0009276)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009277	HP:0009277	Contracture of the metacarpophalangeal joint of the 4th finger	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.