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: C0338474
Disease: Central nervous system demyelination
Central nervous system demyelination 		52 0 3 3.9E-02 0 0
CUI: C0221151
Disease: Projectile vomiting
Projectile vomiting 		1 0 1 3.7E-02 0 0
CUI: C0265978
Disease: Collagen nevus of skin
Collagen nevus of skin 		1 0 1 3.7E-02 0 0
CUI: C0349661
Disease: Glial tumor of brain (disorder)
Glial tumor of brain (disorder) 		1 0 1 3.7E-02 0 0
CUI: C0394004
Disease: Congenital non-progressive ataxia
Congenital non-progressive ataxia 		1 0 1 3.7E-02 0 0
CUI: C0476241
Disease: Delayed developmental milestones
Delayed developmental milestones 		1 0 1 3.7E-02 0 0
CUI: C0496920
Disease: Neoplasm of uncertain or unknown behavior of ovary
Neoplasm of uncertain or unknown behavior of ovary 		29 0 2 3.7E-02 0 0
CUI: C0810006
Disease: Acute cerebrovascular disease
Acute cerebrovascular disease 		1 0 1 3.7E-02 0 0
CUI: C1313977
Disease: Dental cyst
Dental cyst 		1 0 1 3.7E-02 0 0
CUI: C1332442
Disease: BRCA1 Syndrome
BRCA1 Syndrome 		1 0 1 3.7E-02 0 0
CUI: C1838457
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP D1
FANCONI ANEMIA, COMPLEMENTATION GROUP D1 		1 0 1 3.7E-02 0 0
CUI: C1843507
Disease: Hypoplasia of the ventral pons
Hypoplasia of the ventral pons 		1 0 1 3.7E-02 0 0
CUI: C1847725
Disease: SPINOCEREBELLAR ATAXIA 15
SPINOCEREBELLAR ATAXIA 15 		1 0 1 3.7E-02 0 0
CUI: C1850053
Disease: Pelizaeus-Merzbacher-like disease, autosomal recessive, 2
Pelizaeus-Merzbacher-like disease, autosomal recessive, 2 		1 4 1 3.7E-02 1 7.7E-02
CUI: C1856974
Disease: PONTOCEREBELLAR HYPOPLASIA TYPE 4 (disorder)
PONTOCEREBELLAR HYPOPLASIA TYPE 4 (disorder) 		1 0 1 3.7E-02 0 0
CUI: C1857762
Disease: Olivopontocerebellar hypoplasia, fetal-onset
Olivopontocerebellar hypoplasia, fetal-onset 		1 0 1 3.7E-02 0 0
CUI: C1867617
Disease: Hypertrophy of skin of soles
Hypertrophy of skin of soles 		1 0 1 3.7E-02 0 0
CUI: C2585231
Disease: Qualitative platelet disorder
Qualitative platelet disorder 		1 0 1 3.7E-02 0 0
CUI: C2675521
Disease: BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 		1 0 1 3.7E-02 0 0
CUI: C2675522
Disease: OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 		1 0 1 3.7E-02 0 0
CUI: C2676465
Disease: Pontocerebellar Hypoplasia Type 2C
Pontocerebellar Hypoplasia Type 2C 		1 0 1 3.7E-02 0 0
CUI: C2677903
Disease: Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia 		1 0 1 3.7E-02 0 0
CUI: C2751641
Disease: GLIOMA SUSCEPTIBILITY 3
GLIOMA SUSCEPTIBILITY 3 		1 0 1 3.7E-02 0 0
CUI: C3150546
Disease: PANCREATIC CANCER, SUSCEPTIBILITY TO, 2
PANCREATIC CANCER, SUSCEPTIBILITY TO, 2 		1 0 1 3.7E-02 0 0
CUI: C3554209
Disease: Congenital pontocerebellar hypoplasia type 8
Congenital pontocerebellar hypoplasia type 8 		1 0 1 3.7E-02 0 0