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: C0080178
Disease: Spina Bifida
Spina Bifida 		130 58 17 0.12 6 9.7E-02
CUI: C0031157
Disease: Peritonsillar Abscess
Peritonsillar Abscess 		10 0 4 0.11 0 0
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele 		72 23 9 9.6E-02 2 6.5E-02
CUI: C4551722
Disease: Encephalocele
Encephalocele 		21 4 4 8.3E-02 1 7.7E-02
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		24 4 4 7.8E-02 1 7.7E-02
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects 		291 122 23 7.7E-02 8 6.5E-02
CUI: C0002888
Disease: Anemia, Megaloblastic
Anemia, Megaloblastic 		16 1 3 6.8E-02 1 1.0E-01
CUI: C4024948
Disease: Anterior encephalocele
Anterior encephalocele 		2 5 2 6.5E-02 3 0.25
CUI: C0027932
Disease: Neurotic Disorders
Neurotic Disorders 		4 0 2 6.1E-02 0 0
CUI: C4021813
Disease: Oral cleft
Oral cleft 		24 7 3 5.8E-02 2 0.13
CUI: C0086133
Disease: Depressive Syndrome
Depressive Syndrome 		6 3 2 5.7E-02 1 8.3E-02
CUI: C0011573
Disease: Endogenous depression
Endogenous depression 		7 0 2 5.6E-02 0 0
CUI: C1861537
Disease: OROFACIAL CLEFT 1
OROFACIAL CLEFT 1 		27 0 3 5.5E-02 0 0
CUI: C3826462
Disease: Depression in children
Depression in children 		8 0 2 5.4E-02 0 0
CUI: C0152426
Disease: Craniorachischisis
Craniorachischisis 		11 0 2 5.0E-02 0 0
CUI: C4083008
Disease: Guillain-Barre Syndrome, Familial
Guillain-Barre Syndrome, Familial 		53 0 4 5.0E-02 0 0
CUI: C0085106
Disease: Familial benign pemphigus
Familial benign pemphigus 		33 0 3 4.9E-02 0 0
CUI: C2020625
Disease: Group B Streptococcal Infection
Group B Streptococcal Infection 		55 0 4 4.9E-02 0 0
CUI: C0677660
Disease: Emotional problems
Emotional problems 		13 0 2 4.8E-02 0 0
CUI: C1861502
Disease: COLCHICINE RESISTANCE
COLCHICINE RESISTANCE 		13 0 2 4.8E-02 0 0
CUI: C0037917
Disease: Spina Bifida Cystica
Spina Bifida Cystica 		14 5 2 4.7E-02 1 7.1E-02
CUI: C0346991
Disease: Secondary malignant neoplasm of omentum
Secondary malignant neoplasm of omentum 		14 0 2 4.7E-02 0 0
CUI: C1112459
Disease: Unresectable Hepatocellular Carcinoma
Unresectable Hepatocellular Carcinoma 		14 0 2 4.7E-02 0 0
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
Severe hereditary factor VIII deficiency disease 		37 15 3 4.6E-02 1 4.2E-02
CUI: C0003509
Disease: Aortitis
Aortitis 		15 0 2 4.5E-02 0 0