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: C0585187
Disease: Infected ascites
Infected ascites 		1 0 1 6.7E-02 0 0
CUI: C1535985
Disease: Staphylococcal osteomyelitis
Staphylococcal osteomyelitis 		1 0 1 6.7E-02 0 0
CUI: C1834993
Disease: Prominent supraorbital arches in adult
Prominent supraorbital arches in adult 		1 0 1 6.7E-02 0 0
CUI: C1838779
Disease: Eiken Skeletal Dysplasia
Eiken Skeletal Dysplasia 		1 0 1 6.7E-02 0 0
CUI: C1840365
Disease: King Denborough syndrome
King Denborough syndrome 		1 0 1 6.7E-02 0 0
CUI: C1845108
Disease: Prominent median palatal raphe
Prominent median palatal raphe 		1 0 1 6.7E-02 0 0
CUI: C1845292
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP B
FANCONI ANEMIA, COMPLEMENTATION GROUP B 		1 0 1 6.7E-02 0 0
CUI: C1848600
Disease: Vater Association With Hydrocephalus
Vater Association With Hydrocephalus 		1 0 1 6.7E-02 0 0
CUI: C1861753
Disease: Multiminicore Disease, Moderate, with Hand Involvement
Multiminicore Disease, Moderate, with Hand Involvement 		1 0 1 6.7E-02 0 0
CUI: C1968843
Disease: MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (disorder)
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (disorder) 		1 0 1 6.7E-02 0 0
CUI: C1971810
Disease: Congenital cardiovascular disorder
Congenital cardiovascular disorder 		1 0 1 6.7E-02 0 0
CUI: C2083352
Disease: Rectus femoris muscle atrophy
Rectus femoris muscle atrophy 		1 0 1 6.7E-02 0 0
CUI: C2674259
Disease: NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder)
NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder) 		1 0 1 6.7E-02 0 0
CUI: C2675369
Disease: Chromosome 22q11.2 Microduplication Syndrome
Chromosome 22q11.2 Microduplication Syndrome 		1 0 1 6.7E-02 0 0
CUI: C2751307
Disease: MICROPHTHALMIA, ISOLATED 4 (disorder)
MICROPHTHALMIA, ISOLATED 4 (disorder) 		1 0 1 6.7E-02 0 0
CUI: C2930980
Disease: Malignant hyperthermia susceptibility type 1
Malignant hyperthermia susceptibility type 1 		1 97 1 6.7E-02 1 1.0E-02
CUI: C3531771
Disease: Dextrotransposition of the great arteries
Dextrotransposition of the great arteries 		1 0 1 6.7E-02 0 0
CUI: C3715164
Disease: LEBER CONGENITAL AMAUROSIS 17
LEBER CONGENITAL AMAUROSIS 17 		1 0 1 6.7E-02 0 0
CUI: C3810343
Disease: SACRAL AGENESIS WITH VERTEBRAL ANOMALIES
SACRAL AGENESIS WITH VERTEBRAL ANOMALIES 		1 0 1 6.7E-02 0 0
CUI: C3839990
Disease: Congenital stenosis of nasal pyriform aperture
Congenital stenosis of nasal pyriform aperture 		1 0 1 6.7E-02 0 0
CUI: C4016368
Disease: CENTRAL CORE DISEASE, AUTOSOMAL RECESSIVE
CENTRAL CORE DISEASE, AUTOSOMAL RECESSIVE 		1 0 1 6.7E-02 0 0
CUI: C4016468
Disease: VACTERL ASSOCIATION, X-LINKED
VACTERL ASSOCIATION, X-LINKED 		1 0 1 6.7E-02 0 0
CUI: C4016770
Disease: CONOTRUNCAL ANOMALY FACE SYNDROME/VELOCARDIOFACIAL SYNDROME
CONOTRUNCAL ANOMALY FACE SYNDROME/VELOCARDIOFACIAL SYNDROME 		1 0 1 6.7E-02 0 0
CUI: C4022510
Disease: Cervicomedullary schisis
Cervicomedullary schisis 		1 0 1 6.7E-02 0 0
CUI: C4022693
Disease: Posteriorly placed anus
Posteriorly placed anus 		1 0 1 6.7E-02 0 0