Cognitive impairment (Phenotype)

Synonyms:HP:0002128, HP:0002129, HP:0002302, HP:0002337, HP:0002441, HP:0006972, HP:0006998, HP:0007211, Abnormality of cognition, Cognitive abnormality, Cognitive defects, Cognitive deficits, Cognitive impairment, Intellectual impairment

Id:HP:0100543

Description:Abnormal cognition is characterized by deficits in thinking, reasoning, or remembering.

Results found

Linked to

	Label	Description
	CA2 Gene (Entity type)	carbonic anhydrase 2
	EIF1AY Gene (Entity type)	eukaryotic translation initiation factor 1A Y-linked
	GNAS Gene (Entity type)	GNAS complex locus
	CHI3L1 Gene (Entity type)	chitinase 3 like 1
	TLR4 Gene (Entity type)	toll like receptor 4
	SPP1 Gene (Entity type)	secreted phosphoprotein 1
	ID1 Gene (Entity type)	inhibitor of DNA binding 1
	TFF1 Gene (Entity type)	trefoil factor 1
	CXCL9 Gene (Entity type)	C-X-C motif chemokine ligand 9
	TM4SF1 Gene (Entity type)	transmembrane 4 L six family member 1

CA2

Gene (Entity type)

carbonic anhydrase 2

EIF1AY

Gene (Entity type)

eukaryotic translation initiation factor 1A Y-linked

GNAS

Gene (Entity type)

GNAS complex locus

CHI3L1

Gene (Entity type)

chitinase 3 like 1

TLR4

Gene (Entity type)

toll like receptor 4

SPP1

Gene (Entity type)

secreted phosphoprotein 1

ID1

Gene (Entity type)

inhibitor of DNA binding 1

TFF1

Gene (Entity type)

trefoil factor 1

CXCL9

Gene (Entity type)

C-X-C motif chemokine ligand 9

TM4SF1

Gene (Entity type)

transmembrane 4 L six family member 1

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The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

Consortium

Community

Resources

CFDE Workbench

The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

@CFDE Workbench 2025