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: C0078918
Disease: Albinism, Oculocutaneous
Albinism, Oculocutaneous 		49 0 10 0.12 0 0
CUI: C0079504
Disease: Hermanski-Pudlak Syndrome
Hermanski-Pudlak Syndrome 		70 0 12 0.12 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 8 0.10 0 0
CUI: C0078917
Disease: Albinism, Ocular
Albinism, Ocular 		37 0 7 9.9E-02 0 0
CUI: C2931875
Disease: Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells 		9 0 4 8.7E-02 0 0
CUI: C3887558
Disease: Hemophagocytic Syndrome
Hemophagocytic Syndrome 		25 0 5 8.2E-02 0 0
CUI: C0398794
Disease: Hypopigmentation-immunodeficiency disease
Hypopigmentation-immunodeficiency disease 		14 0 4 7.8E-02 0 0
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder) 		14 0 4 7.8E-02 0 0
CUI: C4316899
Disease: Cystinosis
Cystinosis 		32 0 5 7.4E-02 0 0
CUI: C0151295
Disease: Mononeuritis Multiplex
Mononeuritis Multiplex 		4 0 3 7.1E-02 0 0
CUI: C3888001
Disease: HERMANSKY-PUDLAK SYNDROME 3
HERMANSKY-PUDLAK SYNDROME 3 		5 0 3 7.0E-02 0 0
CUI: C4728047
Disease: Left anterior descending coronary artery occlusion
Left anterior descending coronary artery occlusion 		5 0 3 7.0E-02 0 0
CUI: C1304508
Disease: Spindle cell hemangioma
Spindle cell hemangioma 		68 0 7 6.9E-02 0 0
CUI: C0270985
Disease: Alcohol myopathy
Alcohol myopathy 		6 0 3 6.8E-02 0 0
CUI: C1370868
Disease: Refractory Chronic Myelogenous Leukemia, BCR-ABL1 Positive
Refractory Chronic Myelogenous Leukemia, BCR-ABL1 Positive 		6 0 3 6.8E-02 0 0
CUI: C3888004
Disease: HERMANSKY-PUDLAK SYNDROME 5
HERMANSKY-PUDLAK SYNDROME 5 		6 0 3 6.8E-02 0 0
CUI: C0032197
Disease: Platelet Storage Pool Deficiency
Platelet Storage Pool Deficiency 		22 0 4 6.8E-02 0 0
CUI: C0024291
Disease: Lymphohistiocytosis, Hemophagocytic
Lymphohistiocytosis, Hemophagocytic 		117 0 10 6.8E-02 0 0
CUI: C1876214
Disease: ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT
ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT 		54 0 6 6.7E-02 0 0
CUI: C0018425
Disease: Gyrate Atrophy
Gyrate Atrophy 		8 0 3 6.5E-02 0 0
CUI: C1135188
Disease: Critical illness myopathy
Critical illness myopathy 		8 0 3 6.5E-02 0 0
CUI: C2931206
Disease: Usher syndrome, type 1B
Usher syndrome, type 1B 		8 0 3 6.5E-02 0 0
CUI: C0476237
Disease: Metabolic symptoms
Metabolic symptoms 		9 0 3 6.4E-02 0 0
CUI: C0546483
Disease: Lung cyst
Lung cyst 		9 0 3 6.4E-02 0 0
CUI: C1737261
Disease: Acute myeloid leukaemia progression
Acute myeloid leukaemia progression 		9 0 3 6.4E-02 0 0