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: C0278114
Disease: Paraplegia, Cerebral
Paraplegia, Cerebral
1 0 1 1.00 0 0
CUI: C0278115
Disease: Paraplegia, Spinal
Paraplegia, Spinal
1 0 1 1.00 0 0
CUI: C0452143
Disease: Paraplegia, Flaccid
Paraplegia, Flaccid
1 0 1 1.00 0 0
CUI: C1968845
Disease: Primary Lateral Sclerosis, Adult, 1
Primary Lateral Sclerosis, Adult, 1
1 0 1 1.00 0 0
Cerebellar ataxia associated with quadrupedal gait
1 0 1 1.00 0 0
CUI: C0742191
Disease: Cervical spinal cord atrophy
Cervical spinal cord atrophy
2 0 1 0.50 0 0
CUI: C1832597
Disease: Herniation of intervertebral nuclei
Herniation of intervertebral nuclei
3 0 1 0.33 0 0
ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION
3 0 1 0.33 0 0
CUI: C0017563
Disease: Gingival Diseases
Gingival Diseases
4 0 1 0.25 0 0
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE
4 0 1 0.25 0 0
CUI: C1853249
Disease: SPINOCEREBELLAR ATAXIA 28
SPINOCEREBELLAR ATAXIA 28
4 0 1 0.25 0 0
CUI: C3711370
Disease: Spastic Paraplegia Type 7
Spastic Paraplegia Type 7
5 0 1 0.20 0 0
CUI: C4024929
Disease: Slowed slurred speech
Slowed slurred speech
5 0 1 0.20 0 0
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
6 0 1 0.17 0 0
Hereditary motor and sensory neuropathy with optic atrophy (disorder)
7 0 1 0.14 0 0
CUI: C1838579
Disease: Pseudobulbar signs
Pseudobulbar signs
7 0 1 0.14 0 0
CUI: C3711371
Disease: Spastic Paraplegia Type 4
Spastic Paraplegia Type 4
7 0 1 0.14 0 0
Acute lymphoblastic leukemia recurrent
8 0 1 0.12 0 0
CUI: C4025573
Disease: Increased muscle fatiguability
Increased muscle fatiguability
9 0 1 0.11 0 0
CUI: C4552224
Disease: B-cell aplasia
B-cell aplasia
9 0 1 0.11 0 0
CUI: C0345288
Disease: Liver hyperplasia
Liver hyperplasia
10 0 1 1.0E-01 0 0
CUI: C4072903
Disease: Primary Caesarian section
Primary Caesarian section
11 0 1 9.1E-02 0 0
Refractory Adult Acute Lymphoblastic Leukemia
11 0 1 9.1E-02 0 0
Hypoparathyroidism - autosomal dominant
12 0 1 8.3E-02 0 0
CUI: C0574084
Disease: 3-Methylglutaconic aciduria type 3
3-Methylglutaconic aciduria type 3
12 0 1 8.3E-02 0 0