Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0270972
Disease: Cornelia De Lange Syndrome
Cornelia De Lange Syndrome 		0.900 CausalMutation CLINVAR

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0265563
Disease: Congenital dislocation of radial head
Congenital dislocation of radial head 		0.400 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.130 CausalMutation CLINVAR

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.130 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0003467
Disease: Anxiety
Anxiety 		0.110 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		0.110 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.110 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0025990
Disease: Micrognathism
Micrognathism 		0.110 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0033377
Disease: Ptosis
Ptosis 		0.110 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		0.110 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0085271
Disease: Self-Injurious Behavior
Self-Injurious Behavior 		0.110 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0235833
Disease: Congenital diaphragmatic hernia
Congenital diaphragmatic hernia 		0.110 GeneticVariation CLINVAR

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0235833
Disease: Congenital diaphragmatic hernia
Congenital diaphragmatic hernia 		0.110 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.110 GeneticVariation CLINVAR

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0004106
Disease: Astigmatism
Astigmatism 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0005741
Disease: Blepharitis
Blepharitis 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		0.100 GeneticVariation CLINVAR

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0015300
Disease: Exophthalmos
Exophthalmos 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		0.100 Biomarker HPO