Source: BEFREE ×
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: C1844853
Disease: Brachytelephalangic Chondrodysplasia Punctata
Brachytelephalangic Chondrodysplasia Punctata 		5 0 4 0.29 0 0
CUI: C0282102
Disease: Chondrodysplasia punctata, X-linked dominant type
Chondrodysplasia punctata, X-linked dominant type 		9 0 3 0.16 0 0
CUI: C3669395
Disease: X-Linked Chondrodysplasia Punctata 1
X-Linked Chondrodysplasia Punctata 1 		2 0 2 0.15 0 0
CUI: C0268263
Disease: Multiple Sulfatase Deficiency Disease
Multiple Sulfatase Deficiency Disease 		11 0 3 0.14 0 0
CUI: C0265374
Disease: Warfarin syndrome
Warfarin syndrome 		4 0 2 0.13 0 0
CUI: C0009677
Disease: Congenital macroglossia
Congenital macroglossia 		7 0 2 0.11 0 0
CUI: C0024421
Disease: Macroglossia
Macroglossia 		7 0 2 0.11 0 0
CUI: C0018121
Disease: Gradenigo Syndrome
Gradenigo Syndrome 		1 0 1 7.7E-02 0 0
CUI: C0026686
Disease: Mucocele of salivary gland
Mucocele of salivary gland 		1 0 1 7.7E-02 0 0
CUI: C0153614
Disease: Malignant neoplasm of ureteric orifice
Malignant neoplasm of ureteric orifice 		1 0 1 7.7E-02 0 0
CUI: C0155804
Disease: Acute maxillary sinusitis
Acute maxillary sinusitis 		1 0 1 7.7E-02 0 0
CUI: C0263627
Disease: Calcinosis universalis
Calcinosis universalis 		1 0 1 7.7E-02 0 0
CUI: C0264272
Disease: Purulent rhinitis
Purulent rhinitis 		1 0 1 7.7E-02 0 0
CUI: C0264622
Disease: Psychogenic voice disorder
Psychogenic voice disorder 		1 0 1 7.7E-02 0 0
CUI: C0270709
Disease: Rud Syndrome
Rud Syndrome 		1 0 1 7.7E-02 0 0
CUI: C0302246
Disease: Hexadactyly
Hexadactyly 		1 0 1 7.7E-02 0 0
CUI: C0344787
Disease: Complete atrioventricular septal defect
Complete atrioventricular septal defect 		1 0 1 7.7E-02 0 0
CUI: C0423479
Disease: Ear symptom
Ear symptom 		1 0 1 7.7E-02 0 0
CUI: C0600272
Disease: Morphine Abuse
Morphine Abuse 		1 0 1 7.7E-02 0 0
CUI: C0751124
Disease: Epilepsy, Absence, Atypical
Epilepsy, Absence, Atypical 		1 0 1 7.7E-02 0 0
CUI: C0795812
Disease: Chromosome 4, trisomy 4q
Chromosome 4, trisomy 4q 		1 0 1 7.7E-02 0 0
CUI: C0795868
Disease: Chromosome 18, tetrasomy 18p
Chromosome 18, tetrasomy 18p 		1 0 1 7.7E-02 0 0
CUI: C0795939
Disease: AMINOPTERIN SYNDROME SINE AMINOPTERIN
AMINOPTERIN SYNDROME SINE AMINOPTERIN 		1 0 1 7.7E-02 0 0
CUI: C0796032
Disease: Malpuech facial clefting syndrome
Malpuech facial clefting syndrome 		1 0 1 7.7E-02 0 0
CUI: C1304147
Disease: Retention hyperkeratosis
Retention hyperkeratosis 		1 0 1 7.7E-02 0 0