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: C4317009
Disease: Diverticular Diseases
Diverticular Diseases 		83 0 13 0.16 0 0
CUI: C0039614
Disease: Tetanus
Tetanus 		1 0 1 7.7E-02 0 0
CUI: C0432334
Disease: Inherited cutis laxa
Inherited cutis laxa 		1 0 1 7.7E-02 0 0
CUI: C1305147
Disease: Congenital supravalvular aortic stenosis
Congenital supravalvular aortic stenosis 		1 0 1 7.7E-02 0 0
CUI: C1333502
Disease: extragonadal seminoma
extragonadal seminoma 		1 0 1 7.7E-02 0 0
CUI: C1836182
Disease: Chondrodysplasia, acromesomelic, with genital anomalies
Chondrodysplasia, acromesomelic, with genital anomalies 		1 0 1 7.7E-02 0 0
CUI: C1836187
Disease: Widened proximal tibial metaphyses
Widened proximal tibial metaphyses 		1 0 1 7.7E-02 0 0
CUI: C3276539
Disease: CUTIS LAXA, AUTOSOMAL DOMINANT 1
CUTIS LAXA, AUTOSOMAL DOMINANT 1 		1 0 1 7.7E-02 0 0
CUI: C3278154
Disease: GLUTARIC ACIDEMIA IIA
GLUTARIC ACIDEMIA IIA 		1 0 1 7.7E-02 0 0
CUI: C3279150
Disease: Functional hyposplenism
Functional hyposplenism 		1 0 1 7.7E-02 0 0
CUI: C3887897
Disease: Idiopathic atrophoderma of Pasini and Pierini
Idiopathic atrophoderma of Pasini and Pierini 		1 0 1 7.7E-02 0 0
CUI: C4016797
Disease: INFECTIONS, RECURRENT, ASSOCIATED WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, AND CARDIOVASCULAR MALFORMATIONS
INFECTIONS, RECURRENT, ASSOCIATED WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, AND CARDIOVASCULAR MALFORMATIONS 		1 0 1 7.7E-02 0 0
CUI: C4021302
Disease: Aplasia of the proximal phalanges of the hand
Aplasia of the proximal phalanges of the hand 		1 0 1 7.7E-02 0 0
CUI: C4049455
Disease: Pseudoxanthoma elasticum-like papillary dermal elastolysis
Pseudoxanthoma elasticum-like papillary dermal elastolysis 		1 0 1 7.7E-02 0 0
CUI: C4225183
Disease: BRACHYDACTYLY, TYPE A1, D
BRACHYDACTYLY, TYPE A1, D 		1 0 1 7.7E-02 0 0
CUI: C4225404
Disease: ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE
ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE 		1 0 1 7.7E-02 0 0
CUI: C4324411
Disease: Blood type incompatibility
Blood type incompatibility 		1 0 1 7.7E-02 0 0
CUI: C4703482
Disease: Severe Epstein Barr virus infection
Severe Epstein Barr virus infection 		1 0 1 7.7E-02 0 0
CUI: C4751167
Disease: Late-onset focal dermal elastosis
Late-onset focal dermal elastosis 		1 0 1 7.7E-02 0 0
CUI: C0020701
Disease: Hysteria
Hysteria 		2 0 1 7.1E-02 0 0
CUI: C0038368
Disease: Stomatognathic Diseases
Stomatognathic Diseases 		2 0 1 7.1E-02 0 0
CUI: C0158371
Disease: Acute osteomyelitis
Acute osteomyelitis 		2 0 1 7.1E-02 0 0
CUI: C0262963
Disease: extragonadal germ cell tumor
extragonadal germ cell tumor 		2 0 1 7.1E-02 0 0
CUI: C0268379
Disease: Pseudocholinesterase deficiency
Pseudocholinesterase deficiency 		2 0 1 7.1E-02 0 0
CUI: C0270202
Disease: Hemolytic disease of fetus OR newborn due to ABO immunization
Hemolytic disease of fetus OR newborn due to ABO immunization 		2 0 1 7.1E-02 0 0