DisGeNET - a database of gene-disease associations

Source: INFERRED

Gene: AHI1 ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Gene Full Name

DSI _g

DPI _g

pLI

Disease

Type

Score _gda

EL_gda

EI _gda

N.PMIDs

N.SNPs _gda

First Ref.

LastRef.

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C0232466
Disease:	Feeding difficulties

Feeding difficulties

phenotype

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C0678230
Disease:	Congenital Epicanthus

Congenital Epicanthus

disease

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C0856975
Disease:	Autistic behavior

Autistic behavior

disease

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C1834129
Disease:	Abnormal vertebral morphology

Abnormal vertebral morphology

phenotype

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C1836047
Disease:	Long face

Long face

phenotype

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C1839326
Disease:	Abnormal form of the vertebral bodies

Abnormal form of the vertebral bodies

phenotype

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C1840077
Disease:	Anteverted nostril

Anteverted nostril

phenotype

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C1840379
Disease:	Cerebellar vermis hypoplasia

Cerebellar vermis hypoplasia

phenotype

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C1849367
Disease:	Nasal bridge wide

Nasal bridge wide

phenotype

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C1854113
Disease:	Prominent nasal bridge

Prominent nasal bridge

phenotype

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C0575081
Disease:	Gait abnormality

Gait abnormality

group

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C0520680
Disease:	Sleep Apnea, Central

Sleep Apnea, Central

disease

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C0476397
Disease:	Electroretinogram abnormal

Electroretinogram abnormal

phenotype

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C0239234
Disease:	Low set ears

Low set ears

disease

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C0240063
Disease:	Coloboma of iris

Coloboma of iris

disease

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C0240379
Disease:	Open mouth (finding)

Open mouth (finding)

phenotype

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C0240896
Disease:	Fundus coloboma

Fundus coloboma

disease

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C0241726
Disease:	Delayed ability to walk

Delayed ability to walk

phenotype

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C0266435
Disease:	Congenital hypoplasia of penis

Congenital hypoplasia of penis

disease

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C4554036
Disease:	Nystagmus, CTCAE 5.0

Nystagmus, CTCAE 5.0

phenotype

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C0266551
Disease:	Congenital coloboma of iris

Congenital coloboma of iris

disease

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C0339527
Disease:	Leber Congenital Amaurosis

Leber Congenital Amaurosis

disease

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C1854418
Disease:	Biparietal narrowing

Biparietal narrowing

phenotype

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C1857486
Disease:	Low-set, posteriorly rotated ears

Low-set, posteriorly rotated ears

phenotype

0.100

None

Entrez Id:	54806
Gene Symbol:	AHI1

AHI1

Abelson helper integration site 1

0.513

0.846

1.1E-25

CUI:	C1858120
Disease:	Generalized hypotonia

Generalized hypotonia

phenotype

0.100

None