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

..Starting node
..Diminished ability to concentrate (HP:0031987)

Term ID:

31987

Name:

Diminished ability to concentrate

Synonym:

Concentration problems; Lack of concentration; Poor concentration

Definition:

Being unable to focus one's attention or mental effort on a particular object or activity.

Comments:

Reference:

HP:0031987

Genes and Diseases:

Child Nodes:

Sister Nodes:

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:0031987	HP:0031987	Diminished ability to concentrate	0	DYM CL E G H	54808	21317	ORPHA:239	Dyggve-Melchior-Clausen disease	HP:0040283 - Occasional	65
HP:0031987	HP:0031987	Diminished ability to concentrate	0	EMC10 CL E G H	284361	27609	OMIM:619264	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND VARIABLE SEIZURES; NEDDFAS
HP:0031987	HP:0031987	Diminished ability to concentrate	0	ERF CL E G H	2077	3444	OMIM:600775	Craniosynostosis 4	.	12
HP:0031987	HP:0031987	Diminished ability to concentrate	0	HERC2 CL E G H	8924	4868	OMIM:615516	Mental retardation, autosomal recessive 38	.	38
HP:0031987	HP:0031987	Diminished ability to concentrate	0	POLG CL E G H	5428	9179	OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis	.	464
HP:0031987	HP:0031987	Diminished ability to concentrate	0	SPTBN1 CL E G H	6711	11275	OMIM:619475	DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES; DDISBA
HP:0031987	HP:0031987	Diminished ability to concentrate	0	TBL1X CL E G H	6907	11585	OMIM:301033	Hypothyroidism, congenital, nongoitrous, 8	.	1
HP:0031987	HP:0031987	Diminished ability to concentrate	0	TREX1 CL E G H	11277	12269	OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy	.	56
HP:0031987	HP:0031987	Diminished ability to concentrate	0	TWNK CL E G H	56652	1160	OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis	.	113

Genes (9) :DYM EMC10 ERF HERC2 POLG SPTBN1 TBL1X TREX1 TWNK

Diseases (8) :ORPHA:239 OMIM:619264 OMIM:600775 OMIM:615516 OMIM:607459 OMIM:619475 OMIM:301033 OMIM:192315

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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