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: C2673477
Disease: Hypophosphatasia, Perinatal Lethal
Hypophosphatasia, Perinatal Lethal 		1 0 1 6.2E-02 0 0
CUI: C2673923
Disease: Amelogenesis Imperfecta, Type Ic
Amelogenesis Imperfecta, Type Ic 		1 0 1 6.2E-02 0 0
CUI: C2675858
Disease: Amelogenesis Imperfecta, Hypomaturation Type, Iia2
Amelogenesis Imperfecta, Hypomaturation Type, Iia2 		1 0 1 6.2E-02 0 0
CUI: C2750771
Disease: Amelogenesis Imperfecta, Hypomaturation Type, Iia3
Amelogenesis Imperfecta, Hypomaturation Type, Iia3 		1 0 1 6.2E-02 0 0
CUI: C2930833
Disease: Irritable heart
Irritable heart 		1 0 1 6.2E-02 0 0
CUI: C3553288
Disease: HYPEREKPLEXIA 3
HYPEREKPLEXIA 3 		1 0 1 6.2E-02 0 0
CUI: C4016014
Disease: DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 39, WITH DENTINOGENESIS IMPERFECTA 1
DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 39, WITH DENTINOGENESIS IMPERFECTA 1 		1 0 1 6.2E-02 0 0
CUI: C4023094
Disease: Ectopic ossification in ligament tissue
Ectopic ossification in ligament tissue 		1 0 1 6.2E-02 0 0
CUI: C4023095
Disease: Ectopic ossification in tendon tissue
Ectopic ossification in tendon tissue 		1 0 1 6.2E-02 0 0
CUI: C4023157
Disease: Elevated plasma pyrophosphate
Elevated plasma pyrophosphate 		1 0 1 6.2E-02 0 0
CUI: C4023540
Disease: Hypomature dental enamel
Hypomature dental enamel 		1 0 1 6.2E-02 0 0
CUI: C4024079
Disease: Aplasia/Hypoplasia of the phalanges of the hallux
Aplasia/Hypoplasia of the phalanges of the hallux 		1 0 1 6.2E-02 0 0
CUI: C4024082
Disease: Abnormality of the first metatarsal bone
Abnormality of the first metatarsal bone 		1 0 1 6.2E-02 0 0
CUI: C4025607
Disease: Elevated urine pyrophosphate
Elevated urine pyrophosphate 		1 0 1 6.2E-02 0 0
CUI: C4049050
Disease: Opalescent dentin
Opalescent dentin 		1 0 1 6.2E-02 0 0
CUI: C0232191
Disease: Reflex bradycardia
Reflex bradycardia 		2 0 1 5.9E-02 0 0
CUI: C0399380
Disease: Dentin dyspalsia, Shields type 2
Dentin dyspalsia, Shields type 2 		2 0 1 5.9E-02 0 0
CUI: C0477362
Disease: Other specified extrapyramidal and movement disorders
Other specified extrapyramidal and movement disorders 		2 0 1 5.9E-02 0 0
CUI: C1535893
Disease: Orthostatic intolerance
Orthostatic intolerance 		2 0 1 5.9E-02 0 0
CUI: C1832560
Disease: RIPPLING MUSCLE DISEASE 2 (disorder)
RIPPLING MUSCLE DISEASE 2 (disorder) 		2 0 1 5.9E-02 0 0
CUI: C1852169
Disease: Periapical bone loss
Periapical bone loss 		2 0 1 5.9E-02 0 0
CUI: C1855828
Disease: Vertebral clefting
Vertebral clefting 		2 0 1 5.9E-02 0 0
CUI: C1860202
Disease: Unossified vertebral bodies
Unossified vertebral bodies 		2 0 1 5.9E-02 0 0
CUI: C1969038
Disease: RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder)
RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder) 		2 0 1 5.9E-02 0 0
CUI: C3151303
Disease: Obesity, Hyperphagia, and Developmental Delay
Obesity, Hyperphagia, and Developmental Delay 		2 0 1 5.9E-02 0 0