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: C0034150
Disease: Purpura
Purpura
68 0 22 0.19 0 0
CUI: C1860127
Disease: Impaired T cell function
Impaired T cell function
18 0 14 0.19 0 0
CUI: C0020546
Disease: Hypertensive crisis
Hypertensive crisis
19 0 14 0.19 0 0
CUI: C0078982
Disease: Arhinencephaly
Arhinencephaly
35 0 16 0.18 0 0
CUI: C0685891
Disease: Congenital hypoplasia of thymus
Congenital hypoplasia of thymus
34 0 15 0.17 0 0
CUI: C0221277
Disease: Atypical lymphocyte
Atypical lymphocyte
13 0 11 0.15 0 0
CUI: C4021975
Disease: Abnormality of the tonsils
Abnormality of the tonsils
12 0 10 0.14 0 0
CUI: C2700553
Disease: Omenn Syndrome
Omenn Syndrome
35 0 12 0.13 0 0
CUI: C4024912
Disease: Occipital myelomeningocele
Occipital myelomeningocele
9 0 9 0.13 0 0
CUI: C0243002
Disease: Tricuspid Atresia
Tricuspid Atresia
18 0 10 0.13 0 0
CUI: C0151632
Disease: ESR raised
ESR raised
36 0 12 0.13 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome
12 0 9 0.12 0 0
CUI: C4021161
Disease: Multiple suture craniosynostosis
Multiple suture craniosynostosis
12 0 9 0.12 0 0
CUI: C3163801
Disease: Abnormality of aortic arch
Abnormality of aortic arch
13 0 9 0.12 0 0
Desquamation of skin soon after birth
14 0 9 0.12 0 0
CUI: C0401151
Disease: Chronic diarrhea
Chronic diarrhea
62 0 14 0.12 0 0
CUI: C0431406
Disease: Asymmetric crying face association
Asymmetric crying face association
25 0 10 0.12 0 0
CUI: C1836735
Disease: hypopigmented skin patch
hypopigmented skin patch
123 0 20 0.12 0 0
CUI: C1842680
Disease: Small earlobe
Small earlobe
17 0 9 0.12 0 0
CUI: C0032209
Disease: Platybasia
Platybasia
18 0 9 0.11 0 0
CUI: C0795907
Disease: CONOTRUNCAL ANOMALY FACE SYNDROME
CONOTRUNCAL ANOMALY FACE SYNDROME
18 0 9 0.11 0 0
CUI: C1852470
Disease: Extrapyramidal muscular rigidity
Extrapyramidal muscular rigidity
11 0 8 0.11 0 0
CUI: C0271441
Disease: Chronic otitis media
Chronic otitis media
163 0 23 0.11 0 0
CUI: C0040147
Disease: Thyroiditis
Thyroiditis
104 0 17 0.11 0 0
CUI: C1843517
Disease: Retinal arteriolar tortuosity
Retinal arteriolar tortuosity
23 0 9 0.11 0 0