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: C0730309
Disease: Inherited optic neuropathy
Inherited optic neuropathy 		1 0 1 9.1E-02 0 0
CUI: C0948119
Disease: Ovarian fibrosis
Ovarian fibrosis 		1 0 1 9.1E-02 0 0
CUI: C1275420
Disease: Extra-abdominal fibromatosis
Extra-abdominal fibromatosis 		1 0 1 9.1E-02 0 0
CUI: C1300256
Disease: Thanatophoric dysplasia, type 1
Thanatophoric dysplasia, type 1 		1 4 1 9.1E-02 3 0.17
CUI: C1333117
Disease: Colorectal Tubular Adenoma
Colorectal Tubular Adenoma 		1 0 1 9.1E-02 0 0
CUI: C1333987
Disease: Hereditary Glomangioma
Hereditary Glomangioma 		1 0 1 9.1E-02 0 0
CUI: C1334687
Disease: Megakaryocytic Neoplasm
Megakaryocytic Neoplasm 		1 0 1 9.1E-02 0 0
CUI: C1704219
Disease: Dentinogenic Ghost Cell Tumor
Dentinogenic Ghost Cell Tumor 		1 0 1 9.1E-02 0 0
CUI: C1735375
Disease: Progressive optic neuropathy
Progressive optic neuropathy 		1 0 1 9.1E-02 0 0
CUI: C1851152
Disease: SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS
SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS 		1 1 1 9.1E-02 1 5.9E-02
CUI: C1852267
Disease: OPTIC ATROPHY 1 AND DEAFNESS
OPTIC ATROPHY 1 AND DEAFNESS 		1 0 1 9.1E-02 0 0
CUI: C1859524
Disease: Adductor longus contractures
Adductor longus contractures 		1 0 1 9.1E-02 0 0
CUI: C1861213
Disease: Wide-cupped costochondral junctions
Wide-cupped costochondral junctions 		1 0 1 9.1E-02 0 0
CUI: C1863423
Disease: Lumbar kyphosis in infancy
Lumbar kyphosis in infancy 		1 0 1 9.1E-02 0 0
CUI: C1864852
Disease: CATSHL syndrome
CATSHL syndrome 		1 10 1 9.1E-02 7 0.35
CUI: C1864854
Disease: Broad femoral metaphyses
Broad femoral metaphyses 		1 0 1 9.1E-02 0 0
CUI: C2674171
Disease: Lethal short-limbed short stature
Lethal short-limbed short stature 		1 1 1 9.1E-02 1 5.9E-02
CUI: C2677099
Disease: CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS (disorder)
CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS (disorder) 		1 8 1 9.1E-02 7 0.39
CUI: C2930792
Disease: Familial acanthosis nigricans
Familial acanthosis nigricans 		1 1 1 9.1E-02 1 5.9E-02
CUI: C2930793
Disease: Achondroplastic dwarfism
Achondroplastic dwarfism 		1 0 1 9.1E-02 0 0
CUI: C3151467
Disease: Apolipoprotein C-III Deficiency
Apolipoprotein C-III Deficiency 		1 0 1 9.1E-02 0 0
CUI: C3272759
Disease: Brain Development Abnormality
Brain Development Abnormality 		1 0 1 9.1E-02 0 0
CUI: C3275476
Disease: CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA
CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA 		1 0 1 9.1E-02 0 0
CUI: C3279990
Disease: CANDIDIASIS, FAMILIAL, 7
CANDIDIASIS, FAMILIAL, 7 		1 0 1 9.1E-02 0 0
CUI: C3550873
Disease: Hypoplasia of the calcaneus
Hypoplasia of the calcaneus 		1 0 1 9.1E-02 0 0