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: C1844865
Disease: CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3 (disorder)
CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3 (disorder) 		1 0 1 4.8E-02 0 0
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 0 1 4.8E-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 4.8E-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 4.8E-02 0 0
CUI: C1859817
Disease: 2-AMINOADIPIC 2-OXOADIPIC ACIDURIA
2-AMINOADIPIC 2-OXOADIPIC ACIDURIA 		1 0 1 4.8E-02 0 0
CUI: C1861669
Disease: Charcot-Marie-Tooth disease and deafness
Charcot-Marie-Tooth disease and deafness 		1 0 1 4.8E-02 0 0
CUI: C1861678
Disease: Charcot-Marie-Tooth Disease, Axonal, Type 2a1
Charcot-Marie-Tooth Disease, Axonal, Type 2a1 		1 0 1 4.8E-02 0 0
CUI: C2675074
Disease: Enlarged peripheral nerve
Enlarged peripheral nerve 		1 0 1 4.8E-02 0 0
CUI: C2675191
Disease: Polymicrogyria, Bilateral Occipital
Polymicrogyria, Bilateral Occipital 		1 0 1 4.8E-02 0 0
CUI: C2675491
Disease: AMYOTROPHIC LATERAL SCLEROSIS 11
AMYOTROPHIC LATERAL SCLEROSIS 11 		1 0 1 4.8E-02 0 0
CUI: C2733049
Disease: Alpha ketoadipic aciduria
Alpha ketoadipic aciduria 		1 0 1 4.8E-02 0 0
CUI: C2750035
Disease: Emery-Dreifuss Muscular Dystrophy 3
Emery-Dreifuss Muscular Dystrophy 3 		1 0 1 4.8E-02 0 0
CUI: C2750285
Disease: Progeria Syndrome, Childhood-Onset
Progeria Syndrome, Childhood-Onset 		1 0 1 4.8E-02 0 0
CUI: C2750785
Disease: MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder) 		1 0 1 4.8E-02 0 0
CUI: C2931686
Disease: Charcot-Marie-Tooth disease, Type 1E
Charcot-Marie-Tooth disease, Type 1E 		1 0 1 4.8E-02 0 0
CUI: C3150596
Disease: MONONEUROPATHY OF THE MEDIAN NERVE, MILD
MONONEUROPATHY OF THE MEDIAN NERVE, MILD 		1 0 1 4.8E-02 0 0
CUI: C3277187
Disease: Type 2 muscle fiber predominance
Type 2 muscle fiber predominance 		1 0 1 4.8E-02 0 0
CUI: C3280220
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O 		1 0 1 4.8E-02 0 0
CUI: C3281202
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 13
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 		1 0 1 4.8E-02 0 0
CUI: C3495591
Disease: Charcot-Marie-Tooth Disease, Demyelinating, Type 1e
Charcot-Marie-Tooth Disease, Demyelinating, Type 1e 		1 0 1 4.8E-02 0 0
CUI: C4013648
Disease: POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL
POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL 		1 0 1 4.8E-02 0 0
CUI: C4015029
Disease: CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D
CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D 		1 0 1 4.8E-02 0 0
CUI: C4016028
Disease: DEJERINE-SOTTAS NEUROPATHY, AUTOSOMAL DOMINANT
DEJERINE-SOTTAS NEUROPATHY, AUTOSOMAL DOMINANT 		1 0 1 4.8E-02 0 0
CUI: C4016241
Disease: HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL
HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL 		1 0 1 4.8E-02 0 0
CUI: C4016266
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B, WITH FOCALLY FOLDED MYELIN SHEATHS
CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B, WITH FOCALLY FOLDED MYELIN SHEATHS 		1 0 1 4.8E-02 0 0