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: C0332910
Disease: bilateral agenesis
bilateral agenesis
2 0 2 3.7E-02 0 0
CUI: C0442880
Disease: Periungual fibroma
Periungual fibroma
2 0 2 3.7E-02 0 0
CUI: C0585265
Disease: Hypoglossal Nerve Palsy
Hypoglossal Nerve Palsy
2 0 2 3.7E-02 0 0
CUI: C0853277
Disease: Pseudo-Bartter syndrome
Pseudo-Bartter syndrome
2 0 2 3.7E-02 0 0
Polycystic kidneys, severe infantile with tuberous sclerosis
2 0 2 3.7E-02 0 0
CUI: C1860715
Disease: Giant cell astrocytoma
Giant cell astrocytoma
2 0 2 3.7E-02 0 0
CUI: C0014173
Disease: Endometrial Hyperplasia
Endometrial Hyperplasia
143 0 7 3.7E-02 0 0
CUI: C0014850
Disease: Esophageal Atresia
Esophageal Atresia
59 0 4 3.7E-02 0 0
CUI: C3806218
Disease: Episodic tachypnea
Episodic tachypnea
31 0 3 3.7E-02 0 0
Abnormality of female internal genitalia
31 0 3 3.7E-02 0 0
CUI: C0238399
Disease: Pulmonary lymphangiomyomatosis
Pulmonary lymphangiomyomatosis
3 0 2 3.6E-02 0 0
CUI: C0266003
Disease: Subungual fibroma
Subungual fibroma
3 0 2 3.6E-02 0 0
CUI: C0442872
Disease: Multiple cysts
Multiple cysts
3 0 2 3.6E-02 0 0
CUI: C1842876
Disease: Depressed nasal ridge
Depressed nasal ridge
117 0 6 3.6E-02 0 0
Focal Cortical Dysplasia of Taylor, Type IIa
3 0 2 3.6E-02 0 0
Focal Cortical Dysplasia of Taylor, Type IIb
3 0 2 3.6E-02 0 0
CUI: C1860710
Disease: Achromatic retinal patches
Achromatic retinal patches
3 0 2 3.6E-02 0 0
CUI: C1968958
Disease: Subependymal nodules
Subependymal nodules
3 0 2 3.6E-02 0 0
CUI: C1968959
Disease: Cortical tubers
Cortical tubers
3 0 2 3.6E-02 0 0
CUI: C4021899
Disease: Premature chromatid separation
Premature chromatid separation
3 0 2 3.6E-02 0 0
CUI: C1257958
Disease: Glucose Metabolism Disorders
Glucose Metabolism Disorders
32 0 3 3.6E-02 0 0
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL
61 0 4 3.6E-02 0 0
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
33 0 3 3.6E-02 0 0
Carotid Artery, Internal, Dissection
4 0 2 3.6E-02 0 0
CUI: C1863411
Disease: Retinal hamartoma
Retinal hamartoma
4 0 2 3.6E-02 0 0