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: C0423122
Disease: Ptosis of eyebrow
Ptosis of eyebrow 		1 0 1 0.33 0 0
CUI: C0730322
Disease: Multiple evanescent white dot syndrome
Multiple evanescent white dot syndrome 		5 0 2 0.33 0 0
CUI: C2751493
Disease: Cerebral Amyloid Angiopathy, Gsn-Related
Cerebral Amyloid Angiopathy, Gsn-Related 		1 0 1 0.33 0 0
CUI: C4025413
Disease: Curved fingers
Curved fingers 		1 0 1 0.33 0 0
CUI: C4225416
Disease: MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED
MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED 		1 0 1 0.33 0 0
CUI: C4476855
Disease: 5-minute APGAR score of 5
5-minute APGAR score of 5 		1 0 1 0.33 0 0
CUI: C4476858
Disease: 1-minute APGAR score of 1
1-minute APGAR score of 1 		1 0 1 0.33 0 0
CUI: C4477068
Disease: Abnormality of the periodontium
Abnormality of the periodontium 		1 0 1 0.33 0 0
CUI: C4531077
Disease: Abnormal thyroid hormone level
Abnormal thyroid hormone level 		1 0 1 0.33 0 0
CUI: C0857276
Disease: Patellar subluxation
Patellar subluxation 		2 0 1 0.25 0 0
CUI: C0936273
Disease: Familial Amyloid Polyneuropathy, Type IV
Familial Amyloid Polyneuropathy, Type IV 		2 0 1 0.25 0 0
CUI: C1719316
Disease: Inherited systemic amyloidosis
Inherited systemic amyloidosis 		2 0 1 0.25 0 0
CUI: C4524805
Disease: stage IVA gastric cancer
stage IVA gastric cancer 		2 0 1 0.25 0 0
CUI: C3806746
Disease: MENTAL RETARDATION, X-LINKED 99
MENTAL RETARDATION, X-LINKED 99 		3 0 1 0.20 0 0
CUI: C4024863
Disease: Diffuse skin atrophy
Diffuse skin atrophy 		3 0 1 0.20 0 0
CUI: C4024864
Disease: Depigmentation/hyperpigmentation of skin
Depigmentation/hyperpigmentation of skin 		3 0 1 0.20 0 0
CUI: C4025148
Disease: Hyperextensible thumb
Hyperextensible thumb 		3 0 1 0.20 0 0
CUI: C4025812
Disease: Dermatological manifestations of systemic disorders
Dermatological manifestations of systemic disorders 		3 0 1 0.20 0 0
CUI: C4476761
Disease: Abnormal spleen morphology
Abnormal spleen morphology 		3 0 1 0.20 0 0
CUI: C2609282
Disease: Reticular pseudodrusen
Reticular pseudodrusen 		10 0 2 0.18 0 0
CUI: C4081731
Disease: Hereditary systemic amyloidosis
Hereditary systemic amyloidosis 		10 0 2 0.18 0 0
CUI: C0005742
Disease: Blepharochalasis
Blepharochalasis 		4 0 1 0.17 0 0
CUI: C1628319
Disease: Lattice corneal dystrophy Type II
Lattice corneal dystrophy Type II 		4 4 1 0.17 1 0.25
CUI: C2939149
Disease: Amyloid of cornea
Amyloid of cornea 		4 5 1 0.17 1 0.20
CUI: C4023402
Disease: Regional abnormality of skin
Regional abnormality of skin 		4 0 1 0.17 0 0