Source: CLINVAR ×
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: C0027888
Disease: Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathies 		1 0 1 4.2E-02 0 0
CUI: C0033300
Disease: Progeria
Progeria 		1 20 1 4.2E-02 2 2.9E-02
CUI: C0034933
Disease: Reflex, Abnormal
Reflex, Abnormal 		1 0 1 4.2E-02 0 0
CUI: C0042928
Disease: Vocal Cord Paralysis
Vocal Cord Paralysis 		1 1 1 4.2E-02 1 1.9E-02
CUI: C0079035
Disease: Bradyarrhythmia (disorder)
Bradyarrhythmia (disorder) 		1 0 1 4.2E-02 0 0
CUI: C0154681
Disease: Anterior Horn Cell Disease
Anterior Horn Cell Disease 		1 0 1 4.2E-02 0 0
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder) 		1 5 1 4.2E-02 1 1.8E-02
CUI: C0235025
Disease: Peripheral motor neuropathy
Peripheral motor neuropathy 		1 0 1 4.2E-02 0 0
CUI: C0264906
Disease: Second degree atrioventricular block
Second degree atrioventricular block 		1 0 1 4.2E-02 0 0
CUI: C0265280
Disease: Spondylometaphyseal dysplasia, Kozlowski type
Spondylometaphyseal dysplasia, Kozlowski type 		1 6 1 4.2E-02 1 1.8E-02
CUI: C0265281
Disease: Metatropic dwarfism
Metatropic dwarfism 		1 12 1 4.2E-02 1 1.6E-02
CUI: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
Charcot-Marie-Tooth Disease, Type Ia (disorder) 		1 0 1 4.2E-02 0 0
CUI: C0270912
Disease: Charcot-Marie-Tooth Disease, Type Ib
Charcot-Marie-Tooth Disease, Type Ib 		1 40 1 4.2E-02 3 3.4E-02
CUI: C0392777
Disease: Poikiloderma
Poikiloderma 		1 0 1 4.2E-02 0 0
CUI: C0393807
Disease: Hereditary motor and sensory neuropathy with optic atrophy (disorder)
Hereditary motor and sensory neuropathy with optic atrophy (disorder) 		1 10 1 4.2E-02 1 1.6E-02
CUI: C0393808
Disease: Charcot-Marie-Tooth disease, X-linked, 1
Charcot-Marie-Tooth disease, X-linked, 1 		1 0 1 4.2E-02 0 0
CUI: C0393814
Disease: Hereditary liability to pressure palsies
Hereditary liability to pressure palsies 		1 0 1 4.2E-02 0 0
CUI: C0393818
Disease: Congenital hypomyelinating neuropathy
Congenital hypomyelinating neuropathy 		1 0 1 4.2E-02 0 0
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss 		1 0 1 4.2E-02 0 0
CUI: C0410190
Disease: Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder) 		1 0 1 4.2E-02 0 0
CUI: C0426901
Disease: Short leg
Short leg 		1 0 1 4.2E-02 0 0
CUI: C0432227
Disease: Brachyolmia Type 3
Brachyolmia Type 3 		1 3 1 4.2E-02 1 1.9E-02
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis 		1 8 1 4.2E-02 1 1.7E-02
CUI: C0751335
Disease: Scapuloperoneal Form of Spinal Muscular Atrophy
Scapuloperoneal Form of Spinal Muscular Atrophy 		1 4 1 4.2E-02 4 7.7E-02
CUI: C0751336
Disease: Distal Muscular Dystrophies
Distal Muscular Dystrophies 		1 0 1 4.2E-02 0 0