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: C0270150
Disease: Perinatal respiratory failure
Perinatal respiratory failure 		1 0 1 7.1E-02 0 0
CUI: C0333072
Disease: Claw-shaped deformity
Claw-shaped deformity 		1 0 1 7.1E-02 0 0
CUI: C1655035
Disease: congenital muscle disorder
congenital muscle disorder 		1 0 1 7.1E-02 0 0
CUI: C1836336
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H 		1 8 1 7.1E-02 3 3.7E-02
CUI: C1842197
Disease: Charcot-Marie-Tooth Disease, Recessive Intermediate A
Charcot-Marie-Tooth Disease, Recessive Intermediate A 		1 7 1 7.1E-02 1 1.2E-02
CUI: C1842984
Disease: Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k
Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k 		1 0 1 7.1E-02 0 0
CUI: C1843247
Disease: Charcot-Marie-Tooth disease, Type 1D (disorder)
Charcot-Marie-Tooth disease, Type 1D (disorder) 		1 0 1 7.1E-02 0 0
CUI: C1858279
Disease: Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma
Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma 		1 0 1 7.1E-02 0 0
CUI: C1858280
Disease: Charcot-Marie-Tooth Neuropathy, Type 4B2, with Early-Onset Glaucoma
Charcot-Marie-Tooth Neuropathy, Type 4B2, with Early-Onset Glaucoma 		1 0 1 7.1E-02 0 0
CUI: C2675191
Disease: Polymicrogyria, Bilateral Occipital
Polymicrogyria, Bilateral Occipital 		1 0 1 7.1E-02 0 0
CUI: C2675491
Disease: AMYOTROPHIC LATERAL SCLEROSIS 11
AMYOTROPHIC LATERAL SCLEROSIS 11 		1 6 1 7.1E-02 2 2.5E-02
CUI: C2931111
Disease: Myopia, susceptibility to
Myopia, susceptibility to 		1 0 1 7.1E-02 0 0
CUI: C3150596
Disease: MONONEUROPATHY OF THE MEDIAN NERVE, MILD
MONONEUROPATHY OF THE MEDIAN NERVE, MILD 		1 2 1 7.1E-02 2 2.6E-02
CUI: C3540453
Disease: CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F 		1 8 1 7.1E-02 2 2.4E-02
CUI: C3695063
Disease: Charcot-Marie-Tooth disease type 4B3
Charcot-Marie-Tooth disease type 4B3 		1 0 1 7.1E-02 0 0
CUI: C4013648
Disease: POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL
POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL 		1 0 1 7.1E-02 0 0
CUI: C4016028
Disease: DEJERINE-SOTTAS NEUROPATHY, AUTOSOMAL DOMINANT
DEJERINE-SOTTAS NEUROPATHY, AUTOSOMAL DOMINANT 		1 0 1 7.1E-02 0 0
CUI: C4016973
Disease: NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE
NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE 		1 1 1 7.1E-02 1 1.3E-02
CUI: C4024922
Disease: Irregular myelin loops
Irregular myelin loops 		1 0 1 7.1E-02 0 0
CUI: C4024938
Disease: Segmental peripheral demyelination
Segmental peripheral demyelination 		1 0 1 7.1E-02 0 0
CUI: C4024964
Disease: Intraaxonal accumulation of curvilinear autofluorescent lipopigment storage material
Intraaxonal accumulation of curvilinear autofluorescent lipopigment storage material 		1 0 1 7.1E-02 0 0
CUI: C4025322
Disease: Prolonged brainstem auditory evoked potentials
Prolonged brainstem auditory evoked potentials 		1 0 1 7.1E-02 0 0
CUI: C4225250
Disease: SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE 		1 0 1 7.1E-02 0 0
CUI: C4721437
Disease: Charcot-Marie-Tooth disease, Type 4E
Charcot-Marie-Tooth disease, Type 4E 		1 0 1 7.1E-02 0 0
CUI: C4749147
Disease: NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL DOMINANT
NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL DOMINANT 		1 0 1 7.1E-02 0 0