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: C1334720
Disease: Metastatic Malignant Peripheral Nerve Sheath Tumor
Metastatic Malignant Peripheral Nerve Sheath Tumor 		1 0 1 7.1E-02 0 0
CUI: C1840086
Disease: Pectoralis major hypoplasia
Pectoralis major hypoplasia 		1 0 1 7.1E-02 0 0
CUI: C1845243
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE 		1 0 1 7.1E-02 0 0
CUI: C1846478
Disease: Upper limb muscle hypoplasia
Upper limb muscle hypoplasia 		1 0 1 7.1E-02 0 0
CUI: C1847874
Disease: PHACE association
PHACE association 		1 0 1 7.1E-02 0 0
CUI: C1857534
Disease: Postnatal onset growth deficiency
Postnatal onset growth deficiency 		1 0 1 7.1E-02 0 0
CUI: C1858054
Disease: BARDET-BIEDL SYNDROME 6
BARDET-BIEDL SYNDROME 6 		1 0 1 7.1E-02 0 0
CUI: C1859566
Disease: BARDET-BIEDL SYNDROME 8
BARDET-BIEDL SYNDROME 8 		1 0 1 7.1E-02 0 0
CUI: C1859568
Disease: BARDET-BIEDL SYNDROME 10
BARDET-BIEDL SYNDROME 10 		1 0 1 7.1E-02 0 0
CUI: C1868170
Disease: Hypoplasia of deltoid muscle
Hypoplasia of deltoid muscle 		1 0 1 7.1E-02 0 0
CUI: C2674727
Disease: ASTROCYTOMA, LOW-GRADE, SOMATIC
ASTROCYTOMA, LOW-GRADE, SOMATIC 		1 0 1 7.1E-02 0 0
CUI: C2675227
Disease: Endocrine-Cerebroosteodysplasia
Endocrine-Cerebroosteodysplasia 		1 0 1 7.1E-02 0 0
CUI: C2699508
Disease: Splenic diffuse red pulp small B-cell lymphoma
Splenic diffuse red pulp small B-cell lymphoma 		1 0 1 7.1E-02 0 0
CUI: C3150715
Disease: RETINITIS PIGMENTOSA 51
RETINITIS PIGMENTOSA 51 		1 0 1 7.1E-02 0 0
CUI: C3150970
Disease: NOONAN SYNDROME 7
NOONAN SYNDROME 7 		1 0 1 7.1E-02 0 0
CUI: C3150971
Disease: LEOPARD SYNDROME 3
LEOPARD SYNDROME 3 		1 0 1 7.1E-02 0 0
CUI: C3275406
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE 		1 0 1 7.1E-02 0 0
CUI: C3714980
Disease: BARDET-BIEDL SYNDROME 17
BARDET-BIEDL SYNDROME 17 		1 0 1 7.1E-02 0 0
CUI: C3806174
Disease: BARDET-BIEDL SYNDROME 18
BARDET-BIEDL SYNDROME 18 		1 0 1 7.1E-02 0 0
CUI: C3809006
Disease: CARDIOFACIOCUTANEOUS SYNDROME 3
CARDIOFACIOCUTANEOUS SYNDROME 3 		1 0 1 7.1E-02 0 0
CUI: C3897744
Disease: recurrent childhood pleomorphic xanthoastrocytoma
recurrent childhood pleomorphic xanthoastrocytoma 		1 0 1 7.1E-02 0 0
CUI: C3897746
Disease: recurrent childhood pilocytic astrocytoma
recurrent childhood pilocytic astrocytoma 		1 0 1 7.1E-02 0 0
CUI: C4016957
Disease: BARDET-BIEDL SYNDROME 1/2, DIGENIC
BARDET-BIEDL SYNDROME 1/2, DIGENIC 		1 0 1 7.1E-02 0 0
CUI: C4017660
Disease: BARDET-BIEDL SYNDROME 6/10, DIGENIC
BARDET-BIEDL SYNDROME 6/10, DIGENIC 		1 0 1 7.1E-02 0 0
CUI: C4020689
Disease: Insertional polydactyly
Insertional polydactyly 		1 0 1 7.1E-02 0 0