Source: HPO

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		disease 0.410 None 1.000 0 0 2009 2017
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C4025716
Disease: Abnormality of the duodenum
Abnormality of the duodenum 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C1384666
Disease: hearing impairment
hearing impairment 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C1306710
Disease: Facial asymmetry
Facial asymmetry 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos 		disease 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		disease 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C0542514
Disease: Blue sclera
Blue sclera 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C0520947
Disease: Clumsiness - motor delay
Clumsiness - motor delay 		disease 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C0456132
Disease: Large fontanelle
Large fontanelle 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear 		disease 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C0424503
Disease: Dysmorphic facies
Dysmorphic facies 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C0423798
Disease: Increased tendency to bruise
Increased tendency to bruise 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C0423113
Disease: Telecanthus
Telecanthus 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C0423110
Disease: Downward slant of palpebral fissure
Downward slant of palpebral fissure 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C1836308
Disease: Generalized joint laxity
Generalized joint laxity 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C1839546
Disease: Microretrognathia
Microretrognathia 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C3554617
Disease: Adducted thumb
Adducted thumb 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C3489393
Disease: Hiatal Hernia
Hiatal Hernia 		disease 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding) 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C3152182
Disease: Anterior chamber anomalies
Anterior chamber anomalies 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C1865014
Disease: Long philtrum
Long philtrum 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		phenotype 0.100 None 0 0
Entrez Id: 113189
Gene Symbol: CHST14
CHST14 		carbohydrate sulfotransferase 14 0.638 0.654 0.45
CUI: C1857485
Disease: Flat forehead
Flat forehead 		phenotype 0.100 None 0 0