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: C0035934
Disease: Rubinstein-Taybi Syndrome
Rubinstein-Taybi Syndrome 		31 0 11 0.20 0 0
CUI: C2674219
Disease: SPHEROCYTOSIS, HEREDITARY, 2
SPHEROCYTOSIS, HEREDITARY, 2 		8 0 5 0.13 0 0
CUI: C0265372
Disease: Fetal hydantoin syndrome
Fetal hydantoin syndrome 		11 0 5 0.12 0 0
CUI: C2825306
Disease: Treatment related leukaemia
Treatment related leukaemia 		30 0 7 0.12 0 0
CUI: C0795940
Disease: Filippi syndrome
Filippi syndrome 		6 0 4 0.11 0 0
CUI: C3887980
Disease: Protanomaly
Protanomaly 		19 0 5 0.10 0 0
CUI: C0036211
Disease: Sarcoma 180
Sarcoma 180 		20 0 5 1.0E-01 0 0
CUI: C0392777
Disease: Poikiloderma
Poikiloderma 		20 0 5 1.0E-01 0 0
CUI: C0457334
Disease: Acute monoblastic leukemia
Acute monoblastic leukemia 		37 0 6 9.1E-02 0 0
CUI: C1858723
Disease: Poikiloderma with Neutropenia
Poikiloderma with Neutropenia 		25 0 5 9.1E-02 0 0
CUI: C4076240
Disease: Chronic kidney disease mineral and bone disorder
Chronic kidney disease mineral and bone disorder 		26 0 5 8.9E-02 0 0
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		29 0 5 8.5E-02 0 0
CUI: C1292780
Disease: Therapy-related myelodysplastic syndrome
Therapy-related myelodysplastic syndrome 		42 0 6 8.5E-02 0 0
CUI: C1096527
Disease: Mosaic trisomy 8 syndrome
Mosaic trisomy 8 syndrome 		4 0 3 8.3E-02 0 0
CUI: C0948391
Disease: Convulsion in childhood
Convulsion in childhood 		5 0 3 8.1E-02 0 0
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		234 0 20 8.0E-02 0 0
CUI: C0242225
Disease: Color blindness
Color blindness 		33 0 5 7.9E-02 0 0
CUI: C0263498
Disease: Premature canities
Premature canities 		33 0 5 7.9E-02 0 0
CUI: C1563697
Disease: Chromosome Instability Syndromes
Chromosome Instability Syndromes 		6 0 3 7.9E-02 0 0
CUI: C1844508
Disease: Large foramen magnum
Large foramen magnum 		6 0 3 7.9E-02 0 0
CUI: C3831784
Disease: Acute monocytic/monoblastic leukemia
Acute monocytic/monoblastic leukemia 		35 0 5 7.7E-02 0 0
CUI: C0024454
Disease: Maffucci Syndrome
Maffucci Syndrome 		8 0 3 7.5E-02 0 0
CUI: C0008928
Disease: Cleidocranial Dysplasia
Cleidocranial Dysplasia 		52 0 6 7.4E-02 0 0
CUI: C1855496
Disease: Contiguous gene syndrome
Contiguous gene syndrome 		52 0 6 7.4E-02 0 0
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		130 0 11 7.1E-02 0 0