Source: BEFREE ×
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0404521
Disease: Infective vaginitis
Infective vaginitis 		18 0 6 0.17 0 0
CUI: C1112211
Disease: Hepatic Infection
Hepatic Infection 		24 0 6 0.14 0 0
CUI: C0037899
Disease: Sphingolipidoses
Sphingolipidoses 		17 0 5 0.14 0 0
CUI: C3714731
Disease: Early childhood caries
Early childhood caries 		30 0 6 0.12 0 0
CUI: C0023521
Disease: Globoid cell leukodystrophy
Globoid cell leukodystrophy 		34 0 6 0.12 0 0
CUI: C0040253
Disease: Tinea of perianal region
Tinea of perianal region 		6 0 3 0.11 0 0
CUI: C1384589
Disease: Tinea cruris
Tinea cruris 		6 0 3 0.11 0 0
CUI: C0268255
Disease: Farber Lipogranulomatosis
Farber Lipogranulomatosis 		7 0 3 0.11 0 0
CUI: C0700345
Disease: Candidiasis, Vulvovaginal
Candidiasis, Vulvovaginal 		56 0 7 9.6E-02 0 0
CUI: C0028064
Disease: Niemann-Pick Diseases
Niemann-Pick Diseases 		22 0 4 9.5E-02 0 0
CUI: C0751560
Disease: Malignant neoplasm tonsil
Malignant neoplasm tonsil 		22 0 4 9.5E-02 0 0
CUI: C0085131
Disease: Gangliosidosis GM1
Gangliosidosis GM1 		13 0 3 8.8E-02 0 0
CUI: C0268252
Disease: Late-Onset Globoid Cell Leukodystrophy
Late-Onset Globoid Cell Leukodystrophy 		2 0 2 8.3E-02 0 0
CUI: C0751273
Disease: Infantile Globoid Cell Leukodystrophy
Infantile Globoid Cell Leukodystrophy 		2 0 2 8.3E-02 0 0
CUI: C0751278
Disease: Metachromatic Leukodystrophy, Infant
Metachromatic Leukodystrophy, Infant 		2 7 2 8.3E-02 3 9.7E-02
CUI: C0751279
Disease: Metachromatic Leukodystrophy, Adult-Type (disorder)
Metachromatic Leukodystrophy, Adult-Type (disorder) 		2 2 2 8.3E-02 2 7.4E-02
CUI: C2673266
Disease: KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY
KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY 		2 0 2 8.3E-02 0 0
CUI: C2713319
Disease: Arylsulfatase A Deficiency
Arylsulfatase A Deficiency 		2 1 2 8.3E-02 1 3.7E-02
CUI: C4024961
Disease: Metachromatic leukodystrophy variant
Metachromatic leukodystrophy variant 		2 0 2 8.3E-02 0 0
CUI: C0006849
Disease: Oral candidiasis
Oral candidiasis 		57 0 6 8.0E-02 0 0
CUI: C0014040
Disease: Encephalitis Lethargica
Encephalitis Lethargica 		3 0 2 8.0E-02 0 0
CUI: C0040252
Disease: Tinea corporis (disorder)
Tinea corporis (disorder) 		3 0 2 8.0E-02 0 0
CUI: C0282492
Disease: Sneddon Syndrome
Sneddon Syndrome 		3 0 2 8.0E-02 0 0
CUI: C1853623
Disease: Fryns-Aftimos Syndrome
Fryns-Aftimos Syndrome 		3 0 2 8.0E-02 0 0
CUI: C0086795
Disease: Pfaundler-Hurler Syndrome
Pfaundler-Hurler Syndrome 		17 0 3 7.9E-02 0 0