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: C1859049
Disease: CCHS WITH HIRSCHSPRUNG DISEASE
CCHS WITH HIRSCHSPRUNG DISEASE 		7 0 5 0.16 0 0
CUI: C2674219
Disease: SPHEROCYTOSIS, HEREDITARY, 2
SPHEROCYTOSIS, HEREDITARY, 2 		8 0 5 0.16 0 0
CUI: C0020440
Disease: Hypercapnia
Hypercapnia 		11 0 5 0.14 0 0
CUI: C3805839
Disease: Central hypoventilation
Central hypoventilation 		16 0 5 0.12 0 0
CUI: C0345244
Disease: Neuronal intestinal dysplasia
Neuronal intestinal dysplasia 		8 0 4 0.12 0 0
CUI: C3203358
Disease: Hypoventilation
Hypoventilation 		28 0 6 0.12 0 0
CUI: C1832160
Disease: Abnormality of temperature regulation
Abnormality of temperature regulation 		19 0 5 0.12 0 0
CUI: C3887980
Disease: Protanomaly
Protanomaly 		19 0 5 0.12 0 0
CUI: C0036211
Disease: Sarcoma 180
Sarcoma 180 		20 0 5 0.11 0 0
CUI: C0035934
Disease: Rubinstein-Taybi Syndrome
Rubinstein-Taybi Syndrome 		31 0 6 0.11 0 0
CUI: C0008928
Disease: Cleidocranial Dysplasia
Cleidocranial Dysplasia 		52 0 8 0.11 0 0
CUI: C1848519
Disease: WAARDENBURG SYNDROME, TYPE 4A
WAARDENBURG SYNDROME, TYPE 4A 		12 0 4 0.11 0 0
CUI: C0242225
Disease: Color blindness
Color blindness 		33 0 6 0.11 0 0
CUI: C0020681
Disease: Sleep-related respiratory failure
Sleep-related respiratory failure 		3 0 3 0.10 0 0
CUI: C0026633
Disease: Mouth Abnormalities
Mouth Abnormalities 		26 0 5 1.0E-01 0 0
CUI: C1257840
Disease: Aganglionosis, Rectosigmoid Colon
Aganglionosis, Rectosigmoid Colon 		15 0 4 1.0E-01 0 0
CUI: C4076240
Disease: Chronic kidney disease mineral and bone disorder
Chronic kidney disease mineral and bone disorder 		26 0 5 1.0E-01 0 0
CUI: C1859569
Disease: BARDET-BIEDL SYNDROME 11
BARDET-BIEDL SYNDROME 11 		5 0 3 9.7E-02 0 0
CUI: C3661523
Disease: Congenital Intestinal Aganglionosis
Congenital Intestinal Aganglionosis 		18 0 4 9.3E-02 0 0
CUI: C2825306
Disease: Treatment related leukaemia
Treatment related leukaemia 		30 0 5 9.3E-02 0 0
CUI: C0524582
Disease: Mulibrey Nanism
Mulibrey Nanism 		7 0 3 9.1E-02 0 0
CUI: C0795858
Disease: Chromosome 15q, trisomy
Chromosome 15q, trisomy 		7 0 3 9.1E-02 0 0
CUI: C0206718
Disease: Ganglioneuroblastoma
Ganglioneuroblastoma 		57 0 7 8.9E-02 0 0
CUI: C1859305
Disease: Cerebellar Ataxia and Hypogonadotropic Hypogonadism
Cerebellar Ataxia and Hypogonadotropic Hypogonadism 		8 0 3 8.8E-02 0 0
CUI: C2608055
Disease: Hereditary Renal Cell Carcinoma
Hereditary Renal Cell Carcinoma 		8 0 3 8.8E-02 0 0