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: C1168239
Disease: Asymmetry of the ears
Asymmetry of the ears 		4 0 2 5.1E-02 0 0
CUI: C1827396
Disease: Refractory infantile spasms
Refractory infantile spasms 		4 0 2 5.1E-02 0 0
CUI: C0600033
Disease: Acquired Kyphoscoliosis
Acquired Kyphoscoliosis 		149 0 9 5.1E-02 0 0
CUI: C2985290
Disease: Fetal Alcohol Spectrum Disorders
Fetal Alcohol Spectrum Disorders 		46 0 4 5.1E-02 0 0
CUI: C0345392
Disease: Congenital kyphoscoliosis
Congenital kyphoscoliosis 		151 0 9 5.0E-02 0 0
CUI: C0268595
Disease: Glutaric aciduria, type 1
Glutaric aciduria, type 1 		5 0 2 5.0E-02 0 0
CUI: C0345394
Disease: Hypoplasia of spine
Hypoplasia of spine 		5 0 2 5.0E-02 0 0
CUI: C0796016
Disease: Microphthalmia, syndromic 1
Microphthalmia, syndromic 1 		5 0 2 5.0E-02 0 0
CUI: C1849950
Disease: Agenesis of maxillary lateral incisor
Agenesis of maxillary lateral incisor 		5 0 2 5.0E-02 0 0
CUI: C1859773
Disease: Microphthalmia, Syndromic 3
Microphthalmia, Syndromic 3 		5 0 2 5.0E-02 0 0
CUI: C4025810
Disease: Abnormal palmar dermatoglyphics
Abnormal palmar dermatoglyphics 		5 0 2 5.0E-02 0 0
CUI: C0241442
Disease: Protrusion of tongue
Protrusion of tongue 		27 0 3 4.9E-02 0 0
CUI: C0575158
Disease: Kyphoscoliosis deformity of spine
Kyphoscoliosis deformity of spine 		155 0 9 4.9E-02 0 0
CUI: C0036980
Disease: Shock, Cardiogenic
Shock, Cardiogenic 		6 0 2 4.9E-02 0 0
CUI: C0576227
Disease: Narrow foot
Narrow foot 		6 0 2 4.9E-02 0 0
CUI: C0796037
Disease: Martsolf syndrome
Martsolf syndrome 		6 0 2 4.9E-02 0 0
CUI: C0858684
Disease: Facial telangiectasia
Facial telangiectasia 		6 0 2 4.9E-02 0 0
CUI: C0085583
Disease: Choreoathetosis
Choreoathetosis 		94 0 6 4.8E-02 0 0
CUI: C0015411
Disease: Eye Manifestations
Eye Manifestations 		7 0 2 4.8E-02 0 0
CUI: C0752244
Disease: Rathke Cleft Cysts
Rathke Cleft Cysts 		7 0 2 4.8E-02 0 0
CUI: C0796225
Disease: Mental Retardation, X-Linked 19
Mental Retardation, X-Linked 19 		7 0 2 4.8E-02 0 0
CUI: C1844820
Disease: Range of joint movement increased
Range of joint movement increased 		30 0 3 4.7E-02 0 0
CUI: C0270742
Disease: Athetoid cerebral palsy
Athetoid cerebral palsy 		8 0 2 4.7E-02 0 0
CUI: C0393698
Disease: Cryptogenic Infantile Spasms
Cryptogenic Infantile Spasms 		8 0 2 4.7E-02 0 0
CUI: C0575897
Disease: Thumb deformity
Thumb deformity 		8 0 2 4.7E-02 0 0