Source: BEFREE ×
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: C0343239
Disease: Benign congenital hypotonia
Benign congenital hypotonia 		11 0 11 1.00 0 0
CUI: C0270971
Disease: Floppy infant syndrome
Floppy infant syndrome 		31 0 11 0.35 0 0
CUI: C4479088
Disease: MYASTHENIC SYNDROME, CONGENITAL, 22
MYASTHENIC SYNDROME, CONGENITAL, 22 		2 0 2 0.18 0 0
CUI: C4755274
Disease: Atypical hypotonia cystinuria syndrome
Atypical hypotonia cystinuria syndrome 		4 0 2 0.15 0 0
CUI: C1848030
Disease: Hypotonia-Cystinuria Syndrome
Hypotonia-Cystinuria Syndrome 		6 0 2 0.13 0 0
CUI: C0752282
Disease: Congenital Structural Myopathy
Congenital Structural Myopathy 		8 0 2 0.12 0 0
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4 		8 0 2 0.12 0 0
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness 		11 0 2 1.0E-01 0 0
CUI: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis 		11 0 2 1.0E-01 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 9.1E-02 0 0
CUI: C0235909
Disease: Impaired psychomotor development
Impaired psychomotor development 		1 0 1 9.1E-02 0 0
CUI: C0268645
Disease: Cystinuria, type 3
Cystinuria, type 3 		1 0 1 9.1E-02 0 0
CUI: C0270150
Disease: Perinatal respiratory failure
Perinatal respiratory failure 		1 0 1 9.1E-02 0 0
CUI: C0427055
Disease: Facial Paresis
Facial Paresis 		13 0 2 9.1E-02 0 0
CUI: C0585006
Disease: Deficiency of enoyl-CoA hydratase
Deficiency of enoyl-CoA hydratase 		1 0 1 9.1E-02 0 0
CUI: C0677600
Disease: Inspiratory stridor
Inspiratory stridor 		1 0 1 9.1E-02 0 0
CUI: C1533628
Disease: Pseudo-Zellweger syndrome
Pseudo-Zellweger syndrome 		1 0 1 9.1E-02 0 0
CUI: C1655035
Disease: congenital muscle disorder
congenital muscle disorder 		1 0 1 9.1E-02 0 0
CUI: C1839332
Disease: Rett Syndrome, Preserved Speech Variant
Rett Syndrome, Preserved Speech Variant 		1 0 1 9.1E-02 0 0
CUI: C1840365
Disease: King Denborough syndrome
King Denborough syndrome 		1 0 1 9.1E-02 0 0
CUI: C1857388
Disease: Cystinuria, Type A
Cystinuria, Type A 		1 0 1 9.1E-02 0 0
CUI: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79 		1 0 1 9.1E-02 0 0
CUI: C1968556
Disease: ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS 		1 0 1 9.1E-02 0 0
CUI: C2875316
Disease: Myotubular (centronuclear) myopathy
Myotubular (centronuclear) myopathy 		1 0 1 9.1E-02 0 0
CUI: C2931847
Disease: Type I familial incomplete male pseudohermaphroditism
Type I familial incomplete male pseudohermaphroditism 		1 0 1 9.1E-02 0 0