Source: CLINVAR ×
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: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary 		1 0 1 9.7E-03 0 0
CUI: C0018621
Disease: Hay fever
Hay fever 		1 0 1 9.7E-03 0 0
CUI: C0020488
Disease: Hypernatremia
Hypernatremia 		1 1 1 9.7E-03 1 7.6E-03
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism 		1 1 1 9.7E-03 1 7.6E-03
CUI: C0023521
Disease: Globoid cell leukodystrophy
Globoid cell leukodystrophy 		1 0 1 9.7E-03 0 0
CUI: C0028866
Disease: Oculomotor Nerve Paralysis
Oculomotor Nerve Paralysis 		1 1 1 9.7E-03 1 7.6E-03
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome 		1 0 1 9.7E-03 0 0
CUI: C0033893
Disease: Tension Headache
Tension Headache 		1 1 1 9.7E-03 1 7.6E-03
CUI: C0037231
Disease: Sjogren-Larsson Syndrome
Sjogren-Larsson Syndrome 		1 9 1 9.7E-03 1 7.2E-03
CUI: C0151572
Disease: Reflex, Corneal, Decreased
Reflex, Corneal, Decreased 		1 0 1 9.7E-03 0 0
CUI: C0152441
Disease: Madelung Deformity
Madelung Deformity 		1 0 1 9.7E-03 0 0
CUI: C0159020
Disease: Convulsions in the newborn
Convulsions in the newborn 		1 0 1 9.7E-03 0 0
CUI: C0175694
Disease: Smith-Lemli-Opitz Syndrome
Smith-Lemli-Opitz Syndrome 		1 84 1 9.7E-03 1 4.7E-03
CUI: C0221061
Disease: Behr syndrome
Behr syndrome 		1 0 1 9.7E-03 0 0
CUI: C0240896
Disease: Fundus coloboma
Fundus coloboma 		1 0 1 9.7E-03 0 0
CUI: C0241521
Disease: Ulnar deviation of hand
Ulnar deviation of hand 		1 0 1 9.7E-03 0 0
CUI: C0264169
Disease: Saddle nose
Saddle nose 		1 0 1 9.7E-03 0 0
CUI: C0267048
Disease: Glossoptosis
Glossoptosis 		1 0 1 9.7E-03 0 0
CUI: C0268262
Disease: Metachromatic Leukodystrophy due to Saposin B Deficiency
Metachromatic Leukodystrophy due to Saposin B Deficiency 		1 6 1 9.7E-03 1 7.4E-03
CUI: C0270724
Disease: Infantile Neuroaxonal Dystrophy
Infantile Neuroaxonal Dystrophy 		1 22 1 9.7E-03 1 6.6E-03
CUI: C0338480
Disease: Common Migraine
Common Migraine 		1 0 1 9.7E-03 0 0
CUI: C0338508
Disease: Optic Atrophy 1
Optic Atrophy 1 		1 0 1 9.7E-03 0 0
CUI: C0344925
Disease: Perimembranous ventricular septal defect
Perimembranous ventricular septal defect 		1 0 1 9.7E-03 0 0
CUI: C0345326
Disease: Congenital phimosis
Congenital phimosis 		1 1 1 9.7E-03 1 7.6E-03
CUI: C0349653
Disease: Congenital disorder of glycosylation type 1A
Congenital disorder of glycosylation type 1A 		1 63 1 9.7E-03 1 5.2E-03