Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Partial Paralysis (Paresis) Vocal Cords
10 0 3 0.18 0 0
CUI: C0040435
Disease: Tooth Diseases
Tooth Diseases
4 0 2 0.17 0 0
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder)
26 0 5 0.16 0 0
CUI: C3661519
Disease: Hereditary Motor Neuronopathy
Hereditary Motor Neuronopathy
12 0 3 0.16 0 0
HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder)
5 0 2 0.15 0 0
CUI: C4024613
Disease: Progressive distal muscular atrophy
Progressive distal muscular atrophy
5 0 2 0.15 0 0
CUI: C0344955
Disease: Ventricular septal hypertrophy
Ventricular septal hypertrophy
8 0 2 0.12 0 0
CUI: C0521532
Disease: Diaphragmatic paresis
Diaphragmatic paresis
8 0 2 0.12 0 0
CUI: C0393907
Disease: Axonal sensorimotor neuropathy
Axonal sensorimotor neuropathy
9 0 2 0.12 0 0
CUI: C4025799
Disease: Ulnar claw
Ulnar claw
9 0 2 0.12 0 0
CUI: C4025830
Disease: Peripheral axonal degeneration
Peripheral axonal degeneration
9 0 2 0.12 0 0
Hereditary Motor and Sensory Neuropathy Type I
19 84 3 0.12 1 1.2E-02
CUI: C1389118
Disease: Peroneal muscle atrophy
Peroneal muscle atrophy
10 2 2 0.11 1 0.33
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy
21 0 3 0.11 0 0
Hereditary motor and sensory neuropathy, types I-IV
21 0 3 0.11 0 0
Peroneal muscular atrophy (axonal type) (hypertrophic type)
21 0 3 0.11 0 0
CUI: C0015708
Disease: Fazio-Londe Syndrome
Fazio-Londe Syndrome
1 0 1 1.0E-01 0 0
CUI: C0234244
Disease: Tissue Pain
Tissue Pain
1 0 1 1.0E-01 0 0
CUI: C0236960
Disease: Dementia due to Parkinson's disease
Dementia due to Parkinson's disease
1 0 1 1.0E-01 0 0
Osteoarthropathy of fingers familial
1 0 1 1.0E-01 0 0
Spondylometaphyseal dysplasia, Kozlowski type
1 0 1 1.0E-01 0 0
CUI: C0265281
Disease: Metatropic dwarfism
Metatropic dwarfism
1 0 1 1.0E-01 0 0
CUI: C0393540
Disease: Childhood Progressive Bulbar Palsy
Childhood Progressive Bulbar Palsy
1 0 1 1.0E-01 0 0
CUI: C0422879
Disease: CNS symptom
CNS symptom
1 0 1 1.0E-01 0 0
CUI: C0432227
Disease: Brachyolmia Type 3
Brachyolmia Type 3
1 0 1 1.0E-01 0 0