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: C0001075
Disease: Achlorhydria
Achlorhydria
1 0 1 3.0E-03 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia
1 9 1 3.0E-03 1 1.6E-03
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
1 0 1 3.0E-03 0 0
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary
1 0 1 3.0E-03 0 0
CUI: C0008073
Disease: Developmental Disabilities
Developmental Disabilities
1 0 1 3.0E-03 0 0
CUI: C0010273
Disease: Craniofacial Dysostosis
Craniofacial Dysostosis
1 0 1 3.0E-03 0 0
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome
1 0 1 3.0E-03 0 0
CUI: C0012736
Disease: Dissecting aortic aneurysm
Dissecting aortic aneurysm
1 0 1 3.0E-03 0 0
CUI: C0016063
Disease: Osteitis Fibrosa Disseminata
Osteitis Fibrosa Disseminata
1 0 1 3.0E-03 0 0
CUI: C0016065
Disease: Polyostotic fibrous dysplasia
Polyostotic fibrous dysplasia
1 0 1 3.0E-03 0 0
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II
1 165 1 3.0E-03 1 1.3E-03
CUI: C0018799
Disease: Heart Diseases
Heart Diseases
1 0 1 3.0E-03 0 0
CUI: C0020039
Disease: Hostility
Hostility
1 0 1 3.0E-03 0 0
CUI: C0020074
Disease: HSAN Type IV
HSAN Type IV
1 0 1 3.0E-03 0 0
CUI: C0020725
Disease: Type II Mucolipidosis
Type II Mucolipidosis
1 0 1 3.0E-03 0 0
CUI: C0023003
Disease: Langer-Giedion Syndrome
Langer-Giedion Syndrome
1 0 1 3.0E-03 0 0
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome
1 0 1 3.0E-03 0 0
CUI: C0024748
Disease: alpha-Mannosidosis
alpha-Mannosidosis
1 62 1 3.0E-03 1 1.5E-03
CUI: C0025210
Disease: Ocular melanosis
Ocular melanosis
1 0 1 3.0E-03 0 0
CUI: C0026707
Disease: Mucopolysaccharidosis IV
Mucopolysaccharidosis IV
1 0 1 3.0E-03 0 0
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
1 764 1 3.0E-03 2 1.5E-03
Hereditary Motor and Sensory Neuropathies
1 0 1 3.0E-03 0 0
CUI: C0030521
Disease: Parathyroid Neoplasms
Parathyroid Neoplasms
1 0 1 3.0E-03 0 0
CUI: C0032339
Disease: Rothmund-Thomson syndrome
Rothmund-Thomson syndrome
1 12 1 3.0E-03 1 1.6E-03
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
1 1 1 3.0E-03 1 1.6E-03