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:
Neurodevelopmental delay (HP:0012758)

Parent Node:
Motor delay (HP:0001270)

..Starting node
..Delayed fine motor development (HP:0010862)

Term ID:

10862

Name:

Delayed fine motor development

Synonym:

Definition:

A type of motor delay characterized by a delay in acquiring the ability to control the fingers and hands.

Comments:

Reference:

HP:0010862

Genes and Diseases:

Child Nodes:

Sister Nodes:

Delayed gross motor development (HP:0002194)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	DiseaseId	Source	Typical association	ClinVar variants	HGNC ID	GeneMIM
HPO disease - gene - phenotype typical associations:
HP:0010862	HP:0010862	Delayed fine motor development	0	CLP1 CL E G H	10978	411493	ORPHA	1	97	16999	608757
HP:0010862	HP:0010862	Delayed fine motor development	0	ITPR1 CL E G H	3708	208513	ORPHA	1	1563	6180	147265
HP:0010862	HP:0010862	Delayed fine motor development	0	TUBB3 CL E G H	10381	300570	ORPHA	1	320	20772	602661
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010862	HP:0010862	Delayed fine motor development	0	CPLX1 CL E G H	10815	352582	ORPHA	0	206	2309	605032
HP:0010862	HP:0010862	Delayed fine motor development	0	TBC1D24 CL E G H	57465	352582	ORPHA	0	893	29203	613577

Genes (5) :CLP1 CPLX1 ITPR1 TBC1D24 TUBB3

Diseases (4) :411493 352582 208513 300570

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.