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: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 7.1E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 7.1E-02 0 0
CUI: C0270709
Disease: Rud Syndrome
Rud Syndrome 		1 0 1 7.1E-02 0 0
CUI: C1304147
Disease: Retention hyperkeratosis
Retention hyperkeratosis 		1 0 1 7.1E-02 0 0
CUI: C1832475
Disease: Deafness, Autosomal Dominant 11
Deafness, Autosomal Dominant 11 		1 16 1 7.1E-02 1 3.8E-02
CUI: C1836027
Disease: Deafness, Autosomal Recessive 23
Deafness, Autosomal Recessive 23 		1 0 1 7.1E-02 0 0
CUI: C1846331
Disease: Juvenile-onset dystonia
Juvenile-onset dystonia 		1 0 1 7.1E-02 0 0
CUI: C1858042
Disease: Becker Nevus Syndrome
Becker Nevus Syndrome 		1 0 1 7.1E-02 0 0
CUI: C1865870
Disease: Deafness, Autosomal Recessive 18
Deafness, Autosomal Recessive 18 		1 0 1 7.1E-02 0 0
CUI: C1865885
Disease: Usher Syndrome, Type IF
Usher Syndrome, Type IF 		1 0 1 7.1E-02 0 0
CUI: C1955858
Disease: Deaf-Blind Syndromes
Deaf-Blind Syndromes 		1 0 1 7.1E-02 0 0
CUI: C1969516
Disease: Aberrant melanosome maturation
Aberrant melanosome maturation 		1 0 1 7.1E-02 0 0
CUI: C3152102
Disease: USH1D/F, CDH23/PCDH15, DIGENIC
USH1D/F, CDH23/PCDH15, DIGENIC 		1 0 1 7.1E-02 0 0
CUI: C3275872
Disease: USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC
USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC 		1 0 1 7.1E-02 0 0
CUI: C4021549
Disease: Euthyroid hyperthyroxinemia
Euthyroid hyperthyroxinemia 		1 0 1 7.1E-02 0 0
CUI: C4023340
Disease: Childhood onset sensorineural hearing impairment
Childhood onset sensorineural hearing impairment 		1 0 1 7.1E-02 0 0
CUI: C4274085
Disease: Syndromic recessive X-linked ichthyosis
Syndromic recessive X-linked ichthyosis 		1 0 1 7.1E-02 0 0
CUI: C0011992
Disease: Infantile Diarrhea
Infantile Diarrhea 		2 0 1 6.7E-02 0 0
CUI: C0040127
Disease: Thyroid Crisis
Thyroid Crisis 		2 0 1 6.7E-02 0 0
CUI: C0266833
Disease: Visceral Myopathy, Familial
Visceral Myopathy, Familial 		2 0 1 6.7E-02 0 0
CUI: C0339282
Disease: Pre-descemet's corneal dystrophy
Pre-descemet's corneal dystrophy 		2 0 1 6.7E-02 0 0
CUI: C1290162
Disease: Disorder of smooth muscle
Disorder of smooth muscle 		2 0 1 6.7E-02 0 0
CUI: C1527298
Disease: Dysentery, Bacillary
Dysentery, Bacillary 		2 0 1 6.7E-02 0 0
CUI: C1832187
Disease: Deafness, Autosomal Dominant 12
Deafness, Autosomal Dominant 12 		2 0 1 6.7E-02 0 0
CUI: C1837819
Disease: Cerebrofrontofacial Syndrome
Cerebrofrontofacial Syndrome 		2 0 1 6.7E-02 0 0