Human Phenotype Ontology

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Hello! Guest! Please Login or Register! Clinician Mode

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 digit morphology (HP:0011297)

Grandparent Node:
Abnormality of the hand (HP:0001155)

Parent Node:
Abnormality of finger (HP:0001167)

..Starting node
..Trident hand (HP:0004060)

Term ID:

4060

Name:

Trident hand

Synonym:

trident abnormality; trident deformity

Definition:

A hand in which the fingers are of nearly equal length and deflected at the first interphalangeal joint, so as to give a forklike shape consisting of separation of the first and second as well as the third and fourth digits.

Comments:

Reference:

HP:0004060

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal 2nd finger morphology (HP:0004100)

Abnormal 3rd finger morphology (HP:0004150)

Abnormal 4th finger morphology (HP:0004188)

Abnormal 5th finger morphology (HP:0004207)

Abnormal finger flexion creases (HP:0006143)

Abnormal finger phalanx morphology (HP:0005918)

Abnormal fingertip morphology (HP:0001211)

Abnormal thumb morphology (HP:0001172)

Aplasia/Hypoplasia of fingers (HP:0006265)

Broad finger (HP:0001500)

Chilblains (HP:0009710)

Curved fingers (HP:0004095)

Deviation of finger (HP:0004097)

Finger dactylitis (HP:0031090)

Finger joint hypermobility (HP:0006094)

Finger swelling (HP:0025131)

Long fingers (HP:0100807)

Macrodactyly of finger (HP:0100746)

Mallet finger (HP:0030771)

Slender finger (HP:0001238)

Spindle-shaped finger (HP:0031092)

Splayed fingers (HP:0030029)

Swan neck-like deformities of the fingers (HP:0006150)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0004060	HP:0004060	Trident hand	0	FGFR3 CL E G H	2261	3690	OMIM:100800	ACHONDROPLASIA	.	145
HP:0004060	HP:0004060	Trident hand	0	FGFR3 CL E G H	2261	3690	ORPHA:15	Achondroplasia	HP:0040282 - Frequent	145
HP:0004060	HP:0004060	Trident hand	0	NEPRO CL E G H	25871	24496	OMIM:618853	ANAUXETIC DYSPLASIA 3; ANXD3

Genes (2) :FGFR3 NEPRO

Diseases (3) :OMIM:100800 ORPHA:15 OMIM:618853

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.

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