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: C0235000
Disease: Gait, Broadened
Gait, Broadened 		4 0 1 0.25 0 0
CUI: C0337210
Disease: Gait, Stumbling
Gait, Stumbling 		4 0 1 0.25 0 0
CUI: C0427128
Disease: Rapid Fatigue of Gait
Rapid Fatigue of Gait 		4 0 1 0.25 0 0
CUI: C0427169
Disease: Marche a Petit Pas
Marche a Petit Pas 		4 0 1 0.25 0 0
CUI: C0427177
Disease: Gait, Hysterical
Gait, Hysterical 		4 0 1 0.25 0 0
CUI: C0751829
Disease: Gait Disorder, Sensorimotor
Gait Disorder, Sensorimotor 		4 0 1 0.25 0 0
CUI: C0751830
Disease: Gait Disorders, Neurologic
Gait Disorders, Neurologic 		4 0 1 0.25 0 0
CUI: C0751831
Disease: Gait, Frontal
Gait, Frontal 		4 0 1 0.25 0 0
CUI: C0751832
Disease: Gait, Widebased
Gait, Widebased 		4 0 1 0.25 0 0
CUI: C1866130
Disease: Rhombencephalosynapsis
Rhombencephalosynapsis 		4 0 1 0.25 0 0
CUI: C1844007
Disease: Corticospinal tract hypoplasia
Corticospinal tract hypoplasia 		5 0 1 0.20 0 0
CUI: C1855350
Disease: Inferior vermis hypoplasia
Inferior vermis hypoplasia 		5 0 1 0.20 0 0
CUI: C0266304
Disease: Double kidney (disorder)
Double kidney (disorder) 		6 0 1 0.17 0 0
CUI: C0266476
Disease: Congenital stenosis of aqueduct of Sylvius
Congenital stenosis of aqueduct of Sylvius 		6 0 1 0.17 0 0
CUI: C4289581
Disease: RELA fusion-positive ependymoma
RELA fusion-positive ependymoma 		6 0 1 0.17 0 0
CUI: C4525059
Disease: Refractory Neuroblastoma
Refractory Neuroblastoma 		6 0 1 0.17 0 0
CUI: C1839264
Disease: SPASTIC PARAPLEGIA 2, X-LINKED (disorder)
SPASTIC PARAPLEGIA 2, X-LINKED (disorder) 		8 0 1 0.12 0 0
CUI: C3887608
Disease: HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1
HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1 		8 0 1 0.12 0 0
CUI: C0796147
Disease: Acrocallosal Syndrome
Acrocallosal Syndrome 		9 0 1 0.11 0 0
CUI: C1337012
Disease: Well-differentiated papillary mesothelioma
Well-differentiated papillary mesothelioma 		9 0 1 0.11 0 0
CUI: C0338457
Disease: Aphasia, Progressive
Aphasia, Progressive 		10 0 1 1.0E-01 0 0
CUI: C0231698
Disease: Gait, Scissors
Gait, Scissors 		12 0 1 8.3E-02 0 0
CUI: C0206675
Disease: Adenomatoid Tumor
Adenomatoid Tumor 		14 0 1 7.1E-02 0 0
CUI: C0018566
Disease: Congenital Hand Deformities
Congenital Hand Deformities 		15 0 1 6.7E-02 0 0
CUI: C0795953
Disease: MASA SYNDROME (disorder)
MASA SYNDROME (disorder) 		16 13 1 6.2E-02 1 7.1E-02