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: C1865596
Disease: Desmosterolosis
Desmosterolosis 		2 0 1 0.17 0 0
CUI: C0263888
Disease: Back disorder
Back disorder 		3 0 1 0.14 0 0
CUI: C1112574
Disease: Granulomatous ileocolitis
Granulomatous ileocolitis 		3 0 1 0.14 0 0
CUI: C1257843
Disease: pseudomembranous colitis
pseudomembranous colitis 		3 0 1 0.14 0 0
CUI: C1846421
Disease: Lathosterolosis
Lathosterolosis 		3 0 1 0.14 0 0
CUI: C4266451
Disease: Fetal abnormality
Fetal abnormality 		3 0 1 0.14 0 0
CUI: C0342783
Disease: Deficiency of butyryl-CoA dehydrogenase
Deficiency of butyryl-CoA dehydrogenase 		21 0 3 0.13 0 0
CUI: C0175694
Disease: Smith-Lemli-Opitz Syndrome
Smith-Lemli-Opitz Syndrome 		30 0 4 0.13 0 0
CUI: C0156173
Disease: Functional diarrhea
Functional diarrhea 		4 0 1 0.12 0 0
CUI: C0238106
Disease: Clostridium difficile colitis
Clostridium difficile colitis 		4 0 1 0.12 0 0
CUI: C1849186
Disease: Severe photosensitivity
Severe photosensitivity 		4 0 1 0.12 0 0
CUI: C4024745
Disease: Aplasia/Hypoplasia affecting the eye
Aplasia/Hypoplasia affecting the eye 		4 0 1 0.12 0 0
CUI: C0031019
Disease: Perianal abscess
Perianal abscess 		5 0 1 0.11 0 0
CUI: C0432040
Disease: Simple syndactyly of toes, first web space
Simple syndactyly of toes, first web space 		5 0 1 0.11 0 0
CUI: C1844605
Disease: Periorbital wrinkles
Periorbital wrinkles 		5 0 1 0.11 0 0
CUI: C1849537
Disease: Persistent open anterior fontanelle
Persistent open anterior fontanelle 		5 0 1 0.11 0 0
CUI: C1857278
Disease: Partial or complete agenesis of corpus callosum
Partial or complete agenesis of corpus callosum 		5 0 1 0.11 0 0
CUI: C4073171
Disease: Elevated plasma acylcarnitine levels
Elevated plasma acylcarnitine levels 		5 0 1 0.11 0 0
CUI: C0265267
Disease: Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 		6 0 1 1.0E-01 0 0
CUI: C0266411
Disease: Septate vagina
Septate vagina 		6 0 1 1.0E-01 0 0
CUI: C3807980
Disease: Apneic episodes in infancy
Apneic episodes in infancy 		6 0 1 1.0E-01 0 0
CUI: C0751771
Disease: Sleep Bruxism
Sleep Bruxism 		7 0 1 9.1E-02 0 0
CUI: C0266249
Disease: Gallbladder anomaly congenital
Gallbladder anomaly congenital 		8 0 1 8.3E-02 0 0
CUI: C0266313
Disease: Allanson Pantzar McLeod syndrome
Allanson Pantzar McLeod syndrome 		8 0 1 8.3E-02 0 0
CUI: C0575897
Disease: Thumb deformity
Thumb deformity 		8 0 1 8.3E-02 0 0