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: C0796046
Disease: Gurrieri Sammito Bellussi syndrome
Gurrieri Sammito Bellussi syndrome
1 0 1 9.1E-02 0 0
CUI: C1517445
Disease: Ganglioneuroblastoma, Nodular
Ganglioneuroblastoma, Nodular
1 0 1 9.1E-02 0 0
CUI: C1856911
Disease: Ivory epiphyses
Ivory epiphyses
1 0 1 9.1E-02 0 0
CUI: C1859458
Disease: Cleft vertebral arch
Cleft vertebral arch
1 0 1 9.1E-02 0 0
CUI: C1859462
Disease: Absent knee epiphyses
Absent knee epiphyses
1 0 1 9.1E-02 0 0
CUI: C1859478
Disease: Hypoplasia of proximal fibula
Hypoplasia of proximal fibula
1 0 1 9.1E-02 0 0
CUI: C2751986
Disease: RETINITIS PIGMENTOSA 42
RETINITIS PIGMENTOSA 42
1 0 1 9.1E-02 0 0
CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL
1 0 1 9.1E-02 0 0
CUI: C4021589
Disease: Absent glenoid fossa
Absent glenoid fossa
1 0 1 9.1E-02 0 0
CUI: C4024619
Disease: Broad femoral head
Broad femoral head
1 0 1 9.1E-02 0 0
Abnormality of the middle phalanx of the 5th finger
1 0 1 9.1E-02 0 0
CUI: C4225188
Disease: MEIER-GORLIN SYNDROME 6
MEIER-GORLIN SYNDROME 6
1 3 1 9.1E-02 1 0.17
CRISPONI/COLD-INDUCED SWEATING SYNDROME 3
1 6 1 9.1E-02 1 0.11
Microcephalic osteodysplastic primordial dwarfism types I and III
1 0 1 9.1E-02 0 0
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY
1 0 1 9.1E-02 0 0
CUI: C4552001
Disease: MEIER-GORLIN SYNDROME 1
MEIER-GORLIN SYNDROME 1
1 0 1 9.1E-02 0 0
CUI: C4725876
Disease: Resectable Neuroblastoma
Resectable Neuroblastoma
1 0 1 9.1E-02 0 0
CUI: C4725878
Disease: Unresectable Neuroblastoma
Unresectable Neuroblastoma
1 0 1 9.1E-02 0 0
CUI: C0431670
Disease: Webbed penis
Webbed penis
2 2 1 8.3E-02 1 0.20
CUI: C0796021
Disease: Lowry Wood syndrome
Lowry Wood syndrome
2 0 1 8.3E-02 0 0
CUI: C1517444
Disease: Ganglioneuroblastoma, Intermixed
Ganglioneuroblastoma, Intermixed
2 0 1 8.3E-02 0 0
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D
2 0 1 8.3E-02 0 0
CUI: C1846059
Disease: Roifman syndrome
Roifman syndrome
2 0 1 8.3E-02 0 0
CUI: C1855177
Disease: Flat glenoid fossa
Flat glenoid fossa
2 0 1 8.3E-02 0 0
CUI: C1857945
Disease: Hyperechogenic pancreas
Hyperechogenic pancreas
2 0 1 8.3E-02 0 0