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: C1836933
Disease: Low-set nipples
Low-set nipples 		9 0 2 0.13 0 0
CUI: C1853102
Disease: Cerebrooculofacioskeletal Syndrome 2
Cerebrooculofacioskeletal Syndrome 2 		1 0 1 0.12 0 0
CUI: C1856089
Disease: Methioninuria
Methioninuria 		1 0 1 0.12 0 0
CUI: C1970808
Disease: Xeroderma Pigmentosum B-Cockayne Syndrome
Xeroderma Pigmentosum B-Cockayne Syndrome 		1 0 1 0.12 0 0
CUI: C2169795
Disease: Recurrent bronchopulmonary infections
Recurrent bronchopulmonary infections 		10 0 2 0.12 0 0
CUI: C2931840
Disease: Aspartylglucosamidase (AGA) deficiency
Aspartylglucosamidase (AGA) deficiency 		1 0 1 0.12 0 0
CUI: C3150344
Disease: HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED
HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED 		1 0 1 0.12 0 0
CUI: C3806565
Disease: XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME
XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME 		1 0 1 0.12 0 0
CUI: C4017301
Disease: ASPARTYLGLUCOSAMINURIA, FINNISH TYPE
ASPARTYLGLUCOSAMINURIA, FINNISH TYPE 		1 0 1 0.12 0 0
CUI: C4017308
Disease: HOMOCYSTINURIA, PYRIDOXINE-NONRESPONSIVE
HOMOCYSTINURIA, PYRIDOXINE-NONRESPONSIVE 		1 0 1 0.12 0 0
CUI: C4020911
Disease: Herpetiform corneal ulceration
Herpetiform corneal ulceration 		1 0 1 0.12 0 0
CUI: C4022419
Disease: Abnormal transferrin saturation
Abnormal transferrin saturation 		1 0 1 0.12 0 0
CUI: C4225344
Disease: TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE
TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE 		1 0 1 0.12 0 0
CUI: C0580413
Disease: Prothrombin time low
Prothrombin time low 		2 0 1 0.11 0 0
CUI: C0854060
Disease: Increased total iron binding capacity
Increased total iron binding capacity 		2 0 1 0.11 0 0
CUI: C1837758
Disease: Bird-like facies
Bird-like facies 		12 0 2 0.11 0 0
CUI: C1848678
Disease: 4-Hydroxyphenylpyruvic aciduria
4-Hydroxyphenylpyruvic aciduria 		2 0 1 0.11 0 0
CUI: C1851443
Disease: Cerebrooculofacioskeletal Syndrome 3
Cerebrooculofacioskeletal Syndrome 3 		2 0 1 0.11 0 0
CUI: C1968561
Disease: Xeroderma Pigmentosum, Type G-Cockayne Syndrome
Xeroderma Pigmentosum, Type G-Cockayne Syndrome 		2 0 1 0.11 0 0
CUI: C2750442
Disease: Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		2 0 1 0.11 0 0
CUI: C2826055
Disease: Mixed phenotype acute leukemia T/myeloid
Mixed phenotype acute leukemia T/myeloid 		2 0 1 0.11 0 0
CUI: C3502110
Disease: Homocystinuria, Pyridoxine-Responsive
Homocystinuria, Pyridoxine-Responsive 		2 0 1 0.11 0 0
CUI: C3672035
Disease: Copper accumulation in liver
Copper accumulation in liver 		2 0 1 0.11 0 0
CUI: C4024949
Disease: Generalized hyperreflexia
Generalized hyperreflexia 		12 0 2 0.11 0 0
CUI: C4525218
Disease: Chicken Hepatoma
Chicken Hepatoma 		2 0 1 0.11 0 0