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: C2751986
Disease: RETINITIS PIGMENTOSA 42
RETINITIS PIGMENTOSA 42 		1 0 1 9.1E-02 0 0
CUI: C3281203
Disease: CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL
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
CUI: C4025406
Disease: Abnormality of the middle phalanx of the 5th finger
Abnormality of the middle phalanx of the 5th finger 		1 0 1 9.1E-02 0 0
CUI: C4025751
Disease: Abnormality of the pancreas
Abnormality of the pancreas 		13 0 2 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
CUI: C4310742
Disease: CRISPONI/COLD-INDUCED SWEATING SYNDROME 3
CRISPONI/COLD-INDUCED SWEATING SYNDROME 3 		1 6 1 9.1E-02 1 0.11
CUI: C4319565
Disease: Microcephalic osteodysplastic primordial dwarfism types I and III
Microcephalic osteodysplastic primordial dwarfism types I and III 		1 0 1 9.1E-02 0 0
CUI: C4540493
Disease: NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY
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: C0231678
Disease: Ulnar deviation of the wrist
Ulnar deviation of the wrist 		14 0 2 8.7E-02 0 0
CUI: C0685776
Disease: Congenital absence of mandible
Congenital absence of mandible 		14 0 2 8.7E-02 0 0
CUI: C1855514
Disease: Severe failure to thrive
Severe failure to thrive 		14 0 2 8.7E-02 0 0
CUI: C1857949
Disease: Prominent metopic ridge
Prominent metopic ridge 		39 2 4 8.7E-02 1 0.20
CUI: C0265563
Disease: Congenital dislocation of radial head
Congenital dislocation of radial head 		27 0 3 8.6E-02 0 0
CUI: C0266009
Disease: Congenital absence of breast
Congenital absence of breast 		15 0 2 8.3E-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
CUI: C1832334
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D
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