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: C0011645
Disease: Dermatosis Papulosa Nigra
Dermatosis Papulosa Nigra 		2 0 2 1.00 0 0
CUI: C0302894
Disease: Stucco keratosis
Stucco keratosis 		2 0 2 1.00 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 0.50 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers 		1 0 1 0.50 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe 		1 0 1 0.50 0 0
CUI: C0158784
Disease: Accessory skeletal muscle
Accessory skeletal muscle 		1 0 1 0.50 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis 		1 0 1 0.50 0 0
CUI: C0495640
Disease: Congenital malformation syndromes involving early overgrowth
Congenital malformation syndromes involving early overgrowth 		1 0 1 0.50 0 0
CUI: C1274594
Disease: Lichenoid actinic keratosis
Lichenoid actinic keratosis 		1 0 1 0.50 0 0
CUI: C1300256
Disease: Thanatophoric dysplasia, type 1
Thanatophoric dysplasia, type 1 		1 0 1 0.50 0 0
CUI: C1334664
Disease: Mediastinal Lymphangioma
Mediastinal Lymphangioma 		1 0 1 0.50 0 0
CUI: C1335389
Disease: Lipomatosis of Nerve
Lipomatosis of Nerve 		1 0 1 0.50 0 0
CUI: C1851152
Disease: SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS
SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS 		1 0 1 0.50 0 0
CUI: C1861213
Disease: Wide-cupped costochondral junctions
Wide-cupped costochondral junctions 		1 0 1 0.50 0 0
CUI: C1863423
Disease: Lumbar kyphosis in infancy
Lumbar kyphosis in infancy 		1 0 1 0.50 0 0
CUI: C1864852
Disease: CATSHL syndrome
CATSHL syndrome 		1 0 1 0.50 0 0
CUI: C1864854
Disease: Broad femoral metaphyses
Broad femoral metaphyses 		1 0 1 0.50 0 0
CUI: C2674171
Disease: Lethal short-limbed short stature
Lethal short-limbed short stature 		1 0 1 0.50 0 0
CUI: C2677099
Disease: CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS (disorder)
CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS (disorder) 		1 0 1 0.50 0 0
CUI: C2751313
Disease: CLAPO Syndrome
CLAPO Syndrome 		1 0 1 0.50 0 0
CUI: C2752042
Disease: Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi
Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 		1 0 1 0.50 0 0
CUI: C2930792
Disease: Familial acanthosis nigricans
Familial acanthosis nigricans 		1 0 1 0.50 0 0
CUI: C2930793
Disease: Achondroplastic dwarfism
Achondroplastic dwarfism 		1 0 1 0.50 0 0
CUI: C3272759
Disease: Brain Development Abnormality
Brain Development Abnormality 		1 0 1 0.50 0 0
CUI: C3550024
Disease: MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME, SOMATIC
MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME, SOMATIC 		1 0 1 0.50 0 0