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: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C4551905
Disease: Pulmonary Venous Return Anomaly
Pulmonary Venous Return Anomaly 		disease 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C1853737
Disease: Prominent occiput
Prominent occiput 		phenotype 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C1849089
Disease: Broad forehead
Broad forehead 		phenotype 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C1846439
Disease: Hypoplasia of the odontoid process
Hypoplasia of the odontoid process 		phenotype 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C1840382
Disease: Abnormality of the ureter
Abnormality of the ureter 		phenotype 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		phenotype 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C1839326
Disease: Abnormal form of the vertebral bodies
Abnormal form of the vertebral bodies 		phenotype 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C1836542
Disease: Depressed nasal bridge
Depressed nasal bridge 		phenotype 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos 		disease 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C1857482
Disease: Slender finger
Slender finger 		phenotype 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears 		phenotype 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C4025900
Disease: Abnormality of female internal genitalia
Abnormality of female internal genitalia 		disease 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C4025309
Disease: Supernumerary vertebral ossification centers
Supernumerary vertebral ossification centers 		disease 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C4025249
Disease: Abnormality of the intervertebral disk
Abnormality of the intervertebral disk 		disease 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C4023616
Disease: Abnormality of immune system physiology
Abnormality of immune system physiology 		phenotype 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		group 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE 		phenotype 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C1968999
Disease: Rib segmentation abnormalities
Rib segmentation abnormalities 		phenotype 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C1865014
Disease: Long philtrum
Long philtrum 		phenotype 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C1261470
Disease: Congenital meningocele
Congenital meningocele 		disease 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C0853877
Disease: Fistula of genitourinary tract
Fistula of genitourinary tract 		disease 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C0848558
Disease: Hypospadias
Hypospadias 		disease 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		disease 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency 		phenotype 0.100 None 0 0
Entrez Id: 3955
Gene Symbol: LFNG
LFNG 		LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase 0.659 0.500 9.8E-02
CUI: C0025958
Disease: Microcephaly
Microcephaly 		disease 0.100 None 0 0