Source: ALL
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: C0599949
Disease: Arterial Stiffness
Arterial Stiffness 		1 0 1 0.33 0 0
CUI: C1280768
Disease: Axenfeld syndrome
Axenfeld syndrome 		1 0 1 0.33 0 0
CUI: C1833563
Disease: Cleft Lip, Congenital Healed
Cleft Lip, Congenital Healed 		1 0 1 0.33 0 0
CUI: C1839928
Disease: IRIS HYPOPLASIA WITH GLAUCOMA
IRIS HYPOPLASIA WITH GLAUCOMA 		1 5 1 0.33 3 0.10
CUI: C1843512
Disease: BRAIN SMALL VESSEL DISEASE WITH HEMORRHAGE
BRAIN SMALL VESSEL DISEASE WITH HEMORRHAGE 		1 0 1 0.33 0 0
CUI: C1862373
Disease: Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities
Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities 		1 0 1 0.33 0 0
CUI: C1864689
Disease: MICROPHTHALMIA, SYNDROMIC 6 (disorder)
MICROPHTHALMIA, SYNDROMIC 6 (disorder) 		1 0 1 0.33 0 0
CUI: C1864825
Disease: Frias syndrome
Frias syndrome 		1 0 1 0.33 0 0
CUI: C1866560
Disease: IRIDOGONIODYSGENESIS, TYPE 1 (disorder)
IRIDOGONIODYSGENESIS, TYPE 1 (disorder) 		1 2 1 0.33 1 3.6E-02
CUI: C1867327
Disease: RETINAL ARTERIES, TORTUOSITY OF
RETINAL ARTERIES, TORTUOSITY OF 		1 0 1 0.33 0 0
CUI: C2675650
Disease: Brain Small Vessel Disease With Axenfeld-Rieger Anomaly
Brain Small Vessel Disease With Axenfeld-Rieger Anomaly 		1 0 1 0.33 0 0
CUI: C2677434
Disease: OROFACIAL CLEFT 11
OROFACIAL CLEFT 11 		1 0 1 0.33 0 0
CUI: C2930808
Disease: Familial vascular leukoencephalopathy
Familial vascular leukoencephalopathy 		1 0 1 0.33 0 0
CUI: C3887633
Disease: Dandy-Walker Syndrome, Familial
Dandy-Walker Syndrome, Familial 		1 0 1 0.33 0 0
CUI: C4013035
Disease: BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES
BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES 		1 0 1 0.33 0 0
CUI: C0795898
Disease: Cleft Palate-Lateral Synechia Syndrome
Cleft Palate-Lateral Synechia Syndrome 		6 0 2 0.29 0 0
CUI: C0221011
Disease: Malignant Atrophic Papulosis
Malignant Atrophic Papulosis 		2 0 1 0.25 0 0
CUI: C0266548
Disease: Axenfeld anomaly (disorder)
Axenfeld anomaly (disorder) 		7 3 2 0.25 1 3.4E-02
CUI: C0270173
Disease: TORCH syndrome
TORCH syndrome 		2 0 1 0.25 0 0
CUI: C0392550
Disease: Hemiplegia, Infantile
Hemiplegia, Infantile 		2 0 1 0.25 0 0
CUI: C0521706
Disease: Unilateral cataract
Unilateral cataract 		2 0 1 0.25 0 0
CUI: C1263853
Disease: Paralytic stroke
Paralytic stroke 		2 0 1 0.25 0 0
CUI: C1335051
Disease: Non-Neoplastic Urinary System Disorder
Non-Neoplastic Urinary System Disorder 		2 0 1 0.25 0 0
CUI: C1867983
Disease: PORENCEPHALY, FAMILIAL
PORENCEPHALY, FAMILIAL 		2 0 1 0.25 0 0
CUI: C2014414
Disease: orthopedic disorders
orthopedic disorders 		2 0 1 0.25 0 0