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: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 6.2E-02 0 0
CUI: C0231246
Disease: Failure to gain weight
Failure to gain weight 		1 2 1 6.2E-02 1 0.33
CUI: C0243057
Disease: Stomatognathic System Abnormalities
Stomatognathic System Abnormalities 		1 0 1 6.2E-02 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 6.2E-02 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus 		1 0 1 6.2E-02 0 0
CUI: C0266692
Disease: Craniopagus
Craniopagus 		1 0 1 6.2E-02 0 0
CUI: C0266878
Disease: External resorption of tooth
External resorption of tooth 		1 0 1 6.2E-02 0 0
CUI: C0270149
Disease: Perinatal respiratory distress
Perinatal respiratory distress 		1 0 1 6.2E-02 0 0
CUI: C0423729
Disease: Chest pain on breathing
Chest pain on breathing 		1 0 1 6.2E-02 0 0
CUI: C0686761
Disease: Lack of bone formation
Lack of bone formation 		1 0 1 6.2E-02 0 0
CUI: C0749794
Disease: Upper Extremity Deformities, Congenital
Upper Extremity Deformities, Congenital 		1 0 1 6.2E-02 0 0
CUI: C0750931
Disease: Arnold-Chiari Malformation, Type III
Arnold-Chiari Malformation, Type III 		1 0 1 6.2E-02 0 0
CUI: C0750932
Disease: Arnold-Chiari Malformation, Type IV
Arnold-Chiari Malformation, Type IV 		1 0 1 6.2E-02 0 0
CUI: C0795829
Disease: Chromosome 8, trisomy 8q
Chromosome 8, trisomy 8q 		1 0 1 6.2E-02 0 0
CUI: C1112616
Disease: Loss of proprioception
Loss of proprioception 		1 0 1 6.2E-02 0 0
CUI: C1411006
Disease: Finger contracture
Finger contracture 		1 0 1 6.2E-02 0 0
CUI: C1834969
Disease: Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly
Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly 		1 0 1 6.2E-02 0 0
CUI: C1835465
Disease: Short stature, postnatal
Short stature, postnatal 		1 3 1 6.2E-02 1 0.25
CUI: C1838416
Disease: CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY
CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY 		1 0 1 6.2E-02 0 0
CUI: C1839125
Disease: Say Meyer syndrome
Say Meyer syndrome 		1 0 1 6.2E-02 0 0
CUI: C1848473
Disease: Whistling appearance
Whistling appearance 		1 0 1 6.2E-02 0 0
CUI: C1860309
Disease: Chin with H-shaped crease
Chin with H-shaped crease 		1 0 1 6.2E-02 0 0
CUI: C1861516
Disease: Cleidocranial Dysplasia, Forme Fruste, With Brachydactyly
Cleidocranial Dysplasia, Forme Fruste, With Brachydactyly 		1 0 1 6.2E-02 0 0
CUI: C1861517
Disease: Abnormal facility in opposing the shoulders
Abnormal facility in opposing the shoulders 		1 0 1 6.2E-02 0 0
CUI: C1861531
Disease: Long second metacarpal
Long second metacarpal 		1 0 1 6.2E-02 0 0