Source: CURATED ×
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: C0026825
Disease: Flaccid Muscle Tone
Flaccid Muscle Tone 		6 0 6 1.00 0 0
CUI: C0427201
Disease: Floppy Muscles
Floppy Muscles 		6 0 6 1.00 0 0
CUI: C0427202
Disease: Muscle Tone Atonic
Muscle Tone Atonic 		6 0 6 1.00 0 0
CUI: C0751330
Disease: Unilateral Hypotonia
Unilateral Hypotonia 		6 0 6 1.00 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		17 579 6 0.35 4 6.5E-03
CUI: C0033922
Disease: Psychomotor Disorders
Psychomotor Disorders 		7 0 2 0.18 0 0
CUI: C0751456
Disease: Developmental Psychomotor Disorders
Developmental Psychomotor Disorders 		7 0 2 0.18 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 0.17 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus 		1 0 1 0.17 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 0.17 0 0
CUI: C0342708
Disease: Gamma aminobutyric acid transaminase deficiency
Gamma aminobutyric acid transaminase deficiency 		1 0 1 0.17 0 0
CUI: C0431886
Disease: Thumb in palm deformity
Thumb in palm deformity 		1 0 1 0.17 0 0
CUI: C0585540
Disease: Myoclonus, Oculopalatal
Myoclonus, Oculopalatal 		1 0 1 0.17 0 0
CUI: C0751348
Disease: Myoclonus Simplex
Myoclonus Simplex 		1 0 1 0.17 0 0
CUI: C0751349
Disease: Myoclonus, Eyelid
Myoclonus, Eyelid 		1 0 1 0.17 0 0
CUI: C0751350
Disease: Myoclonus, Lower Extremity
Myoclonus, Lower Extremity 		1 0 1 0.17 0 0
CUI: C0751351
Disease: Myoclonus, Segmental
Myoclonus, Segmental 		1 0 1 0.17 0 0
CUI: C0751352
Disease: Myoclonus, Nocturnal
Myoclonus, Nocturnal 		1 0 1 0.17 0 0
CUI: C0751353
Disease: Myoclonus, Upper Extremity
Myoclonus, Upper Extremity 		1 0 1 0.17 0 0
CUI: C0751354
Disease: Myoclonus, Action
Myoclonus, Action 		1 0 1 0.17 0 0
CUI: C0751355
Disease: Polymyoclonus
Polymyoclonus 		1 0 1 0.17 0 0
CUI: C1864871
Disease: Chromosome 17q21.31 Deletion Syndrome
Chromosome 17q21.31 Deletion Syndrome 		1 0 1 0.17 0 0
CUI: C1968550
Disease: Mental Retardation, X-Linked, Syndromic 13
Mental Retardation, X-Linked, Syndromic 13 		1 0 1 0.17 0 0
CUI: C1968556
Disease: ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS 		1 0 1 0.17 0 0
CUI: C2749007
Disease: Chromosome Xq28 Duplication Syndrome
Chromosome Xq28 Duplication Syndrome 		1 0 1 0.17 0 0