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: C0037822
Disease: Speech Disorders
Speech Disorders 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0038379
Disease: Strabismus
Strabismus 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.100 CausalMutation CLINVAR

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0042961
Disease: Intestinal Volvulus
Intestinal Volvulus 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0086543
Disease: Cataract
Cataract 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0151526
Disease: Premature Birth
Premature Birth 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0152421
Disease: Macrotia
Macrotia 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0155299
Disease: Coloboma of optic disc
Coloboma of optic disc 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0158761
Disease: Radioulnar Synostosis
Radioulnar Synostosis 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0162298
Disease: Joint stiffness
Joint stiffness 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0162770
Disease: Right Ventricular Hypertrophy
Right Ventricular Hypertrophy 		0.100 GeneticVariation CLINVAR

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0221210
Disease: Congenital malrotation of intestine
Congenital malrotation of intestine 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0221357
Disease: Brachydactyly
Brachydactyly 		0.100 GeneticVariation CLINVAR

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0232939
Disease: Primary physiologic amenorrhea
Primary physiologic amenorrhea 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0234860
Disease: Weak cry
Weak cry 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0238207
Disease: Ectopic kidney
Ectopic kidney 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0239174
Disease: Late tooth eruption
Late tooth eruption 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0239234
Disease: Low set ears
Low set ears 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0239594
Disease: Short finger
Short finger 		0.100 CausalMutation CLINVAR

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0263401
Disease: Cutis marmorata
Cutis marmorata 		0.100 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0265660
Disease: Syndactyly of the toes
Syndactyly of the toes 		0.100 Biomarker HPO