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: C4024949
Disease: Generalized hyperreflexia
Generalized hyperreflexia
12 0 1 8.3E-02 0 0
X-linked agammaglobulinemia with growth hormone deficiency
13 0 1 7.7E-02 0 0
CUI: C0855082
Disease: Refractory Hodgkin Lymphoma
Refractory Hodgkin Lymphoma
13 0 1 7.7E-02 0 0
CUI: C4014650
Disease: Abnormal mitochondrial morphology
Abnormal mitochondrial morphology
13 0 1 7.7E-02 0 0
Refractory Childhood Acute Lymphoblastic Leukemia
13 0 1 7.7E-02 0 0
CUI: C0239831
Disease: Hand muscle weakness
Hand muscle weakness
14 0 1 7.1E-02 0 0
CUI: C0747251
Disease: Progressive spastic paraparesis
Progressive spastic paraparesis
14 0 1 7.1E-02 0 0
HYPERPARATHYROIDISM, NEONATAL SEVERE
14 0 1 7.1E-02 0 0
OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY
14 0 1 7.1E-02 0 0
Refractory Childhood Hodgkin Lymphoma
14 0 1 7.1E-02 0 0
Refractory Acute Lymphoblastic Leukemia
14 0 1 7.1E-02 0 0
CUI: C0282609
Disease: Bone Marrow Neoplasms
Bone Marrow Neoplasms
16 0 1 6.2E-02 0 0
Complicated hereditary spastic paraplegia
16 0 1 6.2E-02 0 0
CUI: C0919976
Disease: Renal cancer metastatic
Renal cancer metastatic
16 0 1 6.2E-02 0 0
CUI: C1335723
Disease: Refractory Follicular Lymphoma
Refractory Follicular Lymphoma
16 0 1 6.2E-02 0 0
CUI: C1854489
Disease: Limb dysmetria
Limb dysmetria
16 0 1 6.2E-02 0 0
CUI: C0751297
Disease: Leptomeningeal Neoplasms
Leptomeningeal Neoplasms
17 0 1 5.9E-02 0 0
CUI: C1854699
Disease: Diffuse cerebellar atrophy
Diffuse cerebellar atrophy
17 0 1 5.9E-02 0 0
CUI: C4725024
Disease: Refractory Leukemia
Refractory Leukemia
17 0 1 5.9E-02 0 0
CUI: C0029131
Disease: Abnormality of the optic nerve
Abnormality of the optic nerve
18 0 1 5.6E-02 0 0
CUI: C0553707
Disease: Malignant epithelioma
Malignant epithelioma
18 0 1 5.6E-02 0 0
CUI: C4025614
Disease: EMG: chronic denervation signs
EMG: chronic denervation signs
18 0 1 5.6E-02 0 0
CUI: C0154682
Disease: Lateral Sclerosis
Lateral Sclerosis
19 0 1 5.3E-02 0 0
CUI: C1720037
Disease: Supranuclear gaze palsy
Supranuclear gaze palsy
19 0 1 5.3E-02 0 0
Autosomal Recessive Hereditary Spastic Paraplegia
20 0 1 5.0E-02 0 0