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: C0003081
Disease: Anisometropia
Anisometropia
1 0 1 1.00 0 0
CUI: C0023801
Disease: Lipomatosis
Lipomatosis
1 0 1 1.00 0 0
Dysplastic gangliocytoma of cerebellum (Lhermitte-Duclos)
1 0 1 1.00 0 0
CUI: C1835047
Disease: MELANOMA, CUTANEOUS MALIGNANT, 1
MELANOMA, CUTANEOUS MALIGNANT, 1
1 0 1 1.00 0 0
CUI: C0085261
Disease: Proteus Syndrome
Proteus Syndrome
2 0 1 0.50 0 0
CUI: C0205822
Disease: Hibernoma
Hibernoma
2 0 1 0.50 0 0
CUI: C0205823
Disease: Pleomorphic Lipoma
Pleomorphic Lipoma
2 0 1 0.50 0 0
CUI: C0265326
Disease: Bannayan-Riley-Ruvalcaba Syndrome
Bannayan-Riley-Ruvalcaba Syndrome
2 1 1 0.50 1 0.17
CUI: C0391826
Disease: Lhermitte-Duclos disease
Lhermitte-Duclos disease
2 58 1 0.50 5 8.5E-02
CUI: C1854416
Disease: MACROCEPHALY/AUTISM SYNDROME
MACROCEPHALY/AUTISM SYNDROME
2 21 1 0.50 5 0.23
CUI: C1866398
Disease: Proteus-Like Syndrome (disorder)
Proteus-Like Syndrome (disorder)
2 56 1 0.50 5 8.8E-02
CUI: C1959582
Disease: PTEN Hamartoma Tumor Syndrome
PTEN Hamartoma Tumor Syndrome
2 193 1 0.50 5 2.6E-02
CUI: C3489413
Disease: Lipomatosis, Multiple
Lipomatosis, Multiple
2 0 1 0.50 0 0
CUI: C0023798
Disease: Lipoma
Lipoma
3 0 1 0.33 0 0
CUI: C0280302
Disease: Squamous cell carcinoma of lip
Squamous cell carcinoma of lip
3 0 1 0.33 0 0
Squamous cell carcinoma of the hypopharynx
3 0 1 0.33 0 0
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
Laryngeal Squamous Cell Carcinoma
3 0 1 0.33 0 0
VACTERL Association With Hydrocephalus
3 7 1 0.33 5 0.62
MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO
3 16 1 0.33 5 0.29
CUI: C3714976
Disease: ACTIVATED PI3K-DELTA SYNDROME
ACTIVATED PI3K-DELTA SYNDROME
3 0 1 0.33 0 0
CUI: C0018916
Disease: Hemangioma
Hemangioma
4 0 1 0.25 0 0
CUI: C0205788
Disease: Histiocytoid hemangioma
Histiocytoid hemangioma
4 0 1 0.25 0 0
CUI: C0205789
Disease: Hemangioma, Intramuscular
Hemangioma, Intramuscular
4 0 1 0.25 0 0
Squamous cell carcinoma of oropharynx
4 0 1 0.25 0 0
CUI: C0332890
Disease: Congenital hemihypertrophy
Congenital hemihypertrophy
4 0 1 0.25 0 0