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: C1855648
Disease: KENNY-CAFFEY SYNDROME, TYPE 1
KENNY-CAFFEY SYNDROME, TYPE 1 		2 0 2 0.67 0 0
CUI: C4316787
Disease: Kenny-Caffey syndrome, type 2
Kenny-Caffey syndrome, type 2 		2 0 2 0.67 0 0
CUI: C1859449
Disease: Thin long bone diaphyses
Thin long bone diaphyses 		3 0 2 0.50 0 0
CUI: C4022179
Disease: Stenosis of the medullary cavity of the long bones
Stenosis of the medullary cavity of the long bones 		3 0 2 0.50 0 0
CUI: C0151940
Disease: Hypocalcemic tetany
Hypocalcemic tetany 		4 0 2 0.40 0 0
CUI: C4025133
Disease: Cortical thickening of long bone diaphyses
Cortical thickening of long bone diaphyses 		4 0 2 0.40 0 0
CUI: C0409896
Disease: Familial chondrocalcinosis
Familial chondrocalcinosis 		1 0 1 0.33 0 0
CUI: C1455734
Disease: Congenital hypoparathyroidism
Congenital hypoparathyroidism 		5 0 2 0.33 0 0
CUI: C1855840
Disease: HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME
HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME 		1 0 1 0.33 0 0
CUI: C1865639
Disease: Gracile bone dysplasia
Gracile bone dysplasia 		1 0 1 0.33 0 0
CUI: C4016917
Disease: CHONDROCALCINOSIS 2, SPORADIC
CHONDROCALCINOSIS 2, SPORADIC 		1 0 1 0.33 0 0
CUI: C4021027
Disease: Abnormality of the medullary cavity of the long bones
Abnormality of the medullary cavity of the long bones 		1 0 1 0.33 0 0
CUI: C4025258
Disease: Polyarticular chondrocalcinosis
Polyarticular chondrocalcinosis 		1 0 1 0.33 0 0
CUI: C4072891
Disease: Abnormal circulating follicle-stimulating hormone level
Abnormal circulating follicle-stimulating hormone level 		1 0 1 0.33 0 0
CUI: C4310667
Disease: ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY
ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY 		1 0 1 0.33 0 0
CUI: C0265291
Disease: Kenny-Caffey syndrome
Kenny-Caffey syndrome 		6 0 2 0.29 0 0
CUI: C1857499
Disease: Bony paranasal bossing
Bony paranasal bossing 		2 0 1 0.25 0 0
CUI: C1867289
Disease: Retinal calcification
Retinal calcification 		2 0 1 0.25 0 0
CUI: C1970617
Disease: Hypoplastic spleen
Hypoplastic spleen 		2 0 1 0.25 0 0
CUI: C2931244
Disease: Craniometaphyseal dysplasia, autosomal recessive type
Craniometaphyseal dysplasia, autosomal recessive type 		2 0 1 0.25 0 0
CUI: C3279807
Disease: CRANIOECTODERMAL DYSPLASIA 3
CRANIOECTODERMAL DYSPLASIA 3 		2 0 1 0.25 0 0
CUI: C3280616
Disease: CRANIOECTODERMAL DYSPLASIA 4
CRANIOECTODERMAL DYSPLASIA 4 		2 0 1 0.25 0 0
CUI: C3554638
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11 		2 0 1 0.25 0 0
CUI: C0265292
Disease: Schwartz-Lelek syndrome
Schwartz-Lelek syndrome 		3 0 1 0.20 0 0
CUI: C0409860
Disease: Rotator cuff tear arthropathy
Rotator cuff tear arthropathy 		3 0 1 0.20 0 0