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: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 3.4E-02 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 3.4E-02 0 0
CUI: C1836326
Disease: Teratoid Tumor, Atypical
Teratoid Tumor, Atypical 		1 0 1 3.4E-02 0 0
CUI: C1836327
Disease: RHABDOID TUMOR PREDISPOSITION SYNDROME 1 (disorder)
RHABDOID TUMOR PREDISPOSITION SYNDROME 1 (disorder) 		1 0 1 3.4E-02 0 0
CUI: C1836336
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H 		1 0 1 3.4E-02 0 0
CUI: C1838868
Disease: Corticospinal tract atrophy
Corticospinal tract atrophy 		1 0 1 3.4E-02 0 0
CUI: C1838916
Disease: ATAXIA AND POLYNEUROPATHY, ADULT-ONSET
ATAXIA AND POLYNEUROPATHY, ADULT-ONSET 		1 0 1 3.4E-02 0 0
CUI: C1839022
Disease: Striatonigral Degeneration, Infantile, Mitochondrial
Striatonigral Degeneration, Infantile, Mitochondrial 		1 0 1 3.4E-02 0 0
CUI: C1843075
Disease: Charcot-Marie-Tooth Disease, Dominant Intermediate D
Charcot-Marie-Tooth Disease, Dominant Intermediate D 		1 0 1 3.4E-02 0 0
CUI: C1843153
Disease: Charcot-Marie-Tooth disease, Type 2J
Charcot-Marie-Tooth disease, Type 2J 		1 0 1 3.4E-02 0 0
CUI: C1843247
Disease: Charcot-Marie-Tooth disease, Type 1D (disorder)
Charcot-Marie-Tooth disease, Type 1D (disorder) 		1 0 1 3.4E-02 0 0
CUI: C1844836
Disease: Ayazi syndrome
Ayazi syndrome 		1 0 1 3.4E-02 0 0
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 0 1 3.4E-02 0 0
CUI: C1863408
Disease: Juvenile posterior subcapsular lenticular opacities
Juvenile posterior subcapsular lenticular opacities 		1 0 1 3.4E-02 0 0
CUI: C1863653
Disease: Unilateral vestibular Schwannoma
Unilateral vestibular Schwannoma 		1 0 1 3.4E-02 0 0
CUI: C1968845
Disease: Primary Lateral Sclerosis, Adult, 1
Primary Lateral Sclerosis, Adult, 1 		1 0 1 3.4E-02 0 0
CUI: C2675074
Disease: Enlarged peripheral nerve
Enlarged peripheral nerve 		1 0 1 3.4E-02 0 0
CUI: C2750035
Disease: Emery-Dreifuss Muscular Dystrophy 3
Emery-Dreifuss Muscular Dystrophy 3 		1 0 1 3.4E-02 0 0
CUI: C2750285
Disease: Progeria Syndrome, Childhood-Onset
Progeria Syndrome, Childhood-Onset 		1 0 1 3.4E-02 0 0
CUI: C2750405
Disease: Malignant Rhabdoid Tumor, Somatic
Malignant Rhabdoid Tumor, Somatic 		1 0 1 3.4E-02 0 0
CUI: C2750785
Disease: MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder) 		1 0 1 3.4E-02 0 0
CUI: C2827432
Disease: Bile Acid Synthesis Defect
Bile Acid Synthesis Defect 		1 0 1 3.4E-02 0 0
CUI: C3150596
Disease: MONONEUROPATHY OF THE MEDIAN NERVE, MILD
MONONEUROPATHY OF THE MEDIAN NERVE, MILD 		1 0 1 3.4E-02 0 0
CUI: C3150754
Disease: GLYCOGEN STORAGE DISEASE XV
GLYCOGEN STORAGE DISEASE XV 		1 0 1 3.4E-02 0 0
CUI: C3272425
Disease: Gastric Schwannoma
Gastric Schwannoma 		1 0 1 3.4E-02 0 0