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: C2745997
Disease: OROFACIODIGITAL SYNDROME VI
OROFACIODIGITAL SYNDROME VI 		11 0 2 0.15 0 0
CUI: C4023916
Disease: Aplasia/Hypoplasia of the tongue
Aplasia/Hypoplasia of the tongue 		19 0 3 0.15 0 0
CUI: C4551631
Disease: Cystic liver disease
Cystic liver disease 		19 0 3 0.15 0 0
CUI: C1857662
Disease: COACH syndrome
COACH syndrome 		4 0 1 0.14 0 0
CUI: C2673885
Disease: Renal hepatic pancreatic dysplasia Dandy Walker cyst
Renal hepatic pancreatic dysplasia Dandy Walker cyst 		4 0 1 0.14 0 0
CUI: C4025719
Disease: Dysgenesis of the cerebellar vermis
Dysgenesis of the cerebellar vermis 		4 0 1 0.14 0 0
CUI: C0232831
Disease: Impairment of urinary concentration
Impairment of urinary concentration 		5 0 1 0.12 0 0
CUI: C1408258
Disease: Kidney damage
Kidney damage 		5 0 1 0.12 0 0
CUI: C1610065
Disease: Urethral atresia
Urethral atresia 		23 0 3 0.12 0 0
CUI: C1836393
Disease: Abnormality of ocular smooth pursuit
Abnormality of ocular smooth pursuit 		5 0 1 0.12 0 0
CUI: C1855677
Disease: Brainstem dysplasia
Brainstem dysplasia 		5 0 1 0.12 0 0
CUI: C4551559
Disease: Senior-Loken Syndrome 1
Senior-Loken Syndrome 1 		5 0 1 0.12 0 0
CUI: C1865060
Disease: Molar tooth sign on MRI
Molar tooth sign on MRI 		35 0 4 0.11 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome 		26 0 3 0.11 0 0
CUI: C4024644
Disease: Multiple small medullary renal cysts
Multiple small medullary renal cysts 		6 0 1 0.11 0 0
CUI: C0266361
Disease: True Hermaphroditism (disorder)
True Hermaphroditism (disorder) 		27 0 3 0.11 0 0
CUI: C1858395
Disease: Tubular atrophy
Tubular atrophy 		17 0 2 0.11 0 0
CUI: C4521759
Disease: Tubular Atrophy Assessment
Tubular Atrophy Assessment 		17 0 2 0.11 0 0
CUI: C0267818
Disease: Bile duct proliferation
Bile duct proliferation 		30 0 3 9.7E-02 0 0
CUI: C3806218
Disease: Episodic tachypnea
Episodic tachypnea 		31 0 3 9.4E-02 0 0
CUI: C0403553
Disease: Renal dysplasia and retinal aplasia (disorder)
Renal dysplasia and retinal aplasia (disorder) 		20 0 2 9.1E-02 0 0
CUI: C1851853
Disease: Midline notch of upper alveolar ridge
Midline notch of upper alveolar ridge 		8 0 1 9.1E-02 0 0
CUI: C2936862
Disease: Bardet-Biedl syndrome 1 (disorder)
Bardet-Biedl syndrome 1 (disorder) 		20 0 2 9.1E-02 0 0
CUI: C0221365
Disease: Double ureter
Double ureter 		34 0 3 8.6E-02 0 0
CUI: C1848595
Disease: Mesoaxial polydactyly
Mesoaxial polydactyly 		9 0 1 8.3E-02 0 0