Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly
2 0 1 0.20 0 0
CUI: C2721580
Disease: Breakthrough cancer pain
Breakthrough cancer pain
2 0 1 0.20 0 0
CUI: C2734068
Disease: Arm span
Arm span
2 0 1 0.20 0 0
Craniometaphyseal dysplasia, autosomal recessive type
2 0 1 0.20 0 0
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26
2 0 1 0.20 0 0
Fifth finger distal phalanx clinodactyly
2 0 1 0.20 0 0
CUI: C4025175
Disease: Congenital alopecia totalis
Congenital alopecia totalis
2 0 1 0.20 0 0
CUI: C0265292
Disease: Schwartz-Lelek syndrome
Schwartz-Lelek syndrome
3 0 1 0.17 0 0
CUI: C1857505
Disease: Club-shaped distal femur
Club-shaped distal femur
3 0 1 0.17 0 0
CUI: C4023731
Disease: 4-5 finger syndactyly
4-5 finger syndactyly
3 0 1 0.17 0 0
ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1
3 0 1 0.17 0 0
CUI: C0016873
Disease: Fused Teeth
Fused Teeth
4 0 1 0.14 0 0
CUI: C0085417
Disease: Epilepsy, Complex Partial
Epilepsy, Complex Partial
4 0 1 0.14 0 0
CUI: C0221215
Disease: Common atrioventricular canal
Common atrioventricular canal
4 0 1 0.14 0 0
CUI: C0264133
Disease: Acquired flat foot
Acquired flat foot
4 0 1 0.14 0 0
Congenital hypoplasia of aortic arch
4 0 1 0.14 0 0
CUI: C0340486
Disease: Induced ventricular tachycardia
Induced ventricular tachycardia
4 0 1 0.14 0 0
CUI: C0344541
Disease: Persistent pupillary membranes
Persistent pupillary membranes
4 0 1 0.14 0 0
CUI: C0740441
Disease: Acute diarrhea
Acute diarrhea
4 0 1 0.14 0 0
Gastrointestinal stromal tumor of small intestine
4 0 1 0.14 0 0
CUI: C1834062
Disease: 3-4 toe syndactyly
3-4 toe syndactyly
4 0 1 0.14 0 0
CUI: C1857501
Disease: Facial hyperostosis
Facial hyperostosis
4 0 1 0.14 0 0
Severe dermatitis, multiple allergies, metabolic wasting syndrome
4 0 1 0.14 0 0
CUI: C0240129
Disease: Knee stiff
Knee stiff
5 0 1 0.12 0 0
CUI: C0340434
Disease: Dystrophic cardiomyopathy
Dystrophic cardiomyopathy
5 0 1 0.12 0 0