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: C4086152
Disease: Childhood Astrocytoma
Childhood Astrocytoma 		0 39 0 0 1 1.9E-02
CUI: C1834692
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA 		1 0 1 8.3E-02 0 0
CUI: C1845095
Disease: DEAFNESS, X-LINKED 5 (disorder)
DEAFNESS, X-LINKED 5 (disorder) 		1 0 1 8.3E-02 0 0
CUI: C1861678
Disease: Charcot-Marie-Tooth Disease, Axonal, Type 2a1
Charcot-Marie-Tooth Disease, Axonal, Type 2a1 		1 0 1 8.3E-02 0 0
CUI: C1970840
Disease: Leukoencephalopathy With Metaphyseal Chondrodysplasia
Leukoencephalopathy With Metaphyseal Chondrodysplasia 		1 0 1 8.3E-02 0 0
CUI: C1970887
Disease: Abnormal middle ear reflexes
Abnormal middle ear reflexes 		1 0 1 8.3E-02 0 0
CUI: C2608087
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB 		1 0 1 8.3E-02 0 0
CUI: C3151753
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6 		1 0 1 8.3E-02 0 0
CUI: C3553656
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB 		1 0 1 8.3E-02 0 0
CUI: C4020736
Disease: Elevated urinary homovanillic acid
Elevated urinary homovanillic acid 		1 0 1 8.3E-02 0 0
CUI: C4021991
Disease: Abnormality of the astrocytes
Abnormality of the astrocytes 		1 0 1 8.3E-02 0 0
CUI: C4280736
Disease: Large knee
Large knee 		1 0 1 8.3E-02 0 0
CUI: C4304400
Disease: X-linked hereditary sensory and autonomic neuropathy with deafness
X-linked hereditary sensory and autonomic neuropathy with deafness 		1 0 1 8.3E-02 0 0
CUI: C4750787
Disease: Autosomal systemic lupus erythematosus
Autosomal systemic lupus erythematosus 		1 0 1 8.3E-02 0 0
CUI: C0000734
Disease: Abdominal mass
Abdominal mass 		2 0 1 7.7E-02 0 0
CUI: C0019937
Disease: Horner Syndrome
Horner Syndrome 		2 0 1 7.7E-02 0 0
CUI: C0549400
Disease: Low APGAR score
Low APGAR score 		2 0 1 7.7E-02 0 0
CUI: C1457873
Disease: Os trigonum disorder
Os trigonum disorder 		2 0 1 7.7E-02 0 0
CUI: C1836752
Disease: Abnormal speech discrimination
Abnormal speech discrimination 		2 0 1 7.7E-02 0 0
CUI: C1837799
Disease: Generalized muscular appearance from birth
Generalized muscular appearance from birth 		2 0 1 7.7E-02 0 0
CUI: C1847896
Disease: Charcot-Marie-Tooth Disease, Dominant Intermediate A
Charcot-Marie-Tooth Disease, Dominant Intermediate A 		2 0 2 0.17 0 0
CUI: C1853247
Disease: SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT
SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT 		2 0 1 7.7E-02 0 0
CUI: C4014700
Disease: ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY
ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY 		2 0 2 0.17 0 0
CUI: C4020735
Disease: Elevated urinary vanillylmandelic acid
Elevated urinary vanillylmandelic acid 		2 0 1 7.7E-02 0 0
CUI: C4021749
Disease: Cystic angiomatosis of bone
Cystic angiomatosis of bone 		2 0 1 7.7E-02 0 0