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: C0011999
Disease: Diastematomyelia
Diastematomyelia
28 0 28 0.74 0 0
CUI: C0152234
Disease: Iniencephaly
Iniencephaly
28 0 28 0.74 0 0
CUI: C0344479
Disease: Spinal Cord Myelodysplasia
Spinal Cord Myelodysplasia
28 0 28 0.74 0 0
CUI: C0027806
Disease: Neurenteric Cyst
Neurenteric Cyst
29 0 28 0.72 0 0
CUI: C0702169
Disease: Acrania
Acrania
31 0 28 0.68 0 0
CUI: C0080218
Disease: Tethered Cord Syndrome
Tethered Cord Syndrome
41 0 28 0.55 0 0
CUI: C0266453
Disease: Exencephaly
Exencephaly
47 0 28 0.49 0 0
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
11 0 8 0.20 0 0
Spina bifida aperta of cervical spine
6 0 6 0.16 0 0
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele
89 0 15 0.13 0 0
CUI: C4024669
Disease: Asymmetry of spinal facet joints
Asymmetry of spinal facet joints
5 0 5 0.13 0 0
CUI: C0002902
Disease: Anencephaly
Anencephaly
59 0 11 0.13 0 0
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects
304 0 38 0.12 0 0
CUI: C0080178
Disease: Spina Bifida
Spina Bifida
179 0 22 0.11 0 0
CUI: C0266508
Disease: Rachischisis
Rachischisis
15 0 5 0.10 0 0
CUI: C0344490
Disease: Sacral agenesis
Sacral agenesis
15 0 5 0.10 0 0
Neural tube defect, folate-sensitive
8 0 4 9.5E-02 0 0
CUI: C0038219
Disease: Status Dysraphicus
Status Dysraphicus
12 0 4 8.7E-02 0 0
CUI: C0431128
Disease: Papillary craniopharyngioma
Papillary craniopharyngioma
65 0 8 8.4E-02 0 0
PHENCYCLIDINE/ARYLCYCLOHEXYLAMINE ABUSE
3 0 3 7.9E-02 0 0
CUI: C1845027
Disease: Spina Bifida, X-Linked
Spina Bifida, X-Linked
5 0 3 7.5E-02 0 0
CUI: C1866559
Disease: Spina Bifida, Folate-Sensitive
Spina Bifida, Folate-Sensitive
5 0 3 7.5E-02 0 0
CUI: C1845026
Disease: Neural tube defects X-linked
Neural tube defects X-linked
6 0 3 7.3E-02 0 0
CUI: C0745730
Disease: Multiple lipomata
Multiple lipomata
38 0 5 7.0E-02 0 0
CUI: C4551722
Disease: Encephalocele
Encephalocele
23 0 4 7.0E-02 0 0