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: C0687751
Disease: Acanthocytosis
Acanthocytosis 		8 0 4 0.36 0 0
CUI: C1328551
Disease: Transfusion associated graft versus host disease
Transfusion associated graft versus host disease 		3 0 2 0.25 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 0.14 0 0
CUI: C0272405
Disease: Functional asplenia
Functional asplenia 		1 0 1 0.14 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 0.14 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 0.14 0 0
CUI: C1860219
Disease: Self-mutilation of tongue and lips due to involuntary movements
Self-mutilation of tongue and lips due to involuntary movements 		1 0 1 0.14 0 0
CUI: C2875313
Disease: Severe [Duchenne] muscular dystrophy
Severe [Duchenne] muscular dystrophy 		1 0 1 0.14 0 0
CUI: C3844818
Disease: Attention Deficit Hyper Activity
Attention Deficit Hyper Activity 		1 0 1 0.14 0 0
CUI: C4016476
Disease: DUCHENNE MUSCULAR DYSTROPHY, MENTAL RETARDATION, AND ABSENCE OF ERG B-WAVE
DUCHENNE MUSCULAR DYSTROPHY, MENTAL RETARDATION, AND ABSENCE OF ERG B-WAVE 		1 0 1 0.14 0 0
CUI: C4016477
Disease: INTERMEDIATE MUSCULAR DYSTROPHY
INTERMEDIATE MUSCULAR DYSTROPHY 		1 0 1 0.14 0 0
CUI: C4022648
Disease: Abnormal muscle fiber dystrophin expression
Abnormal muscle fiber dystrophin expression 		1 0 1 0.14 0 0
CUI: C4479491
Disease: LOPES-MACIEL-RODAN SYNDROME
LOPES-MACIEL-RODAN SYNDROME 		1 0 1 0.14 0 0
CUI: C0522153
Disease: Urine Discoloration
Urine Discoloration 		10 0 2 0.13 0 0
CUI: C0002735
Disease: Oppenheim's Disease
Oppenheim's Disease 		2 0 1 0.12 0 0
CUI: C0026851
Disease: Muscular Dystrophy, Animal
Muscular Dystrophy, Animal 		2 0 1 0.12 0 0
CUI: C0039223
Disease: Tabes Dorsalis
Tabes Dorsalis 		2 0 1 0.12 0 0
CUI: C0156847
Disease: Anaemia, postpartum
Anaemia, postpartum 		2 0 1 0.12 0 0
CUI: C0241705
Disease: Difficulty passing urine
Difficulty passing urine 		2 0 1 0.12 0 0
CUI: C0474702
Disease: Sulfate measurement
Sulfate measurement 		2 0 1 0.12 0 0
CUI: C0948825
Disease: Systremma
Systremma 		2 0 1 0.12 0 0
CUI: C1540600
Disease: Cerebral seizure
Cerebral seizure 		2 0 1 0.12 0 0
CUI: C1860216
Disease: Progressive choreoathetosis
Progressive choreoathetosis 		2 0 1 0.12 0 0
CUI: C4049281
Disease: Pseudogynaecomastia
Pseudogynaecomastia 		2 0 1 0.12 0 0
CUI: C4479476
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60 		2 0 1 0.12 0 0