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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.2E-03
CUI: C0233684
Disease: Delusion of guilt
Delusion of guilt 		0 1 0 0 1 1.2E-03
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		0 31 0 0 1 1.2E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 1.2E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.2E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 1.2E-03
CUI: C0678189
Disease: Hyperlipidemia, group A
Hyperlipidemia, group A 		0 1 0 0 1 1.2E-03
CUI: C0751483
Disease: Familial Retinoblastoma
Familial Retinoblastoma 		0 4 0 0 1 1.2E-03
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder) 		0 1 0 0 1 1.2E-03
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft 		0 2 0 0 2 2.4E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.2E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.2E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 1.2E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 3 3.6E-03
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 1 8.0E-04 0 0
CUI: C3501844
Disease: Familial Nonmedullary Thyroid Cancer
Familial Nonmedullary Thyroid Cancer 		66 0 1 8.0E-04 0 0
CUI: C1843300
Disease: Sparse eyelashes
Sparse eyelashes 		60 0 1 8.1E-04 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 8.1E-04 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		55 0 1 8.1E-04 0 0
CUI: C1395852
Disease: Polydactyly preaxial type 1
Polydactyly preaxial type 1 		49 0 1 8.1E-04 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 1 8.1E-04 0 0
CUI: C1843057
Disease: Calf muscle hypertrophy
Calf muscle hypertrophy 		46 0 1 8.1E-04 0 0
CUI: C0332615
Disease: Myopathic facies
Myopathic facies 		44 0 1 8.2E-04 0 0
CUI: C4551906
Disease: Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		43 0 1 8.2E-04 0 0
CUI: C0234860
Disease: Weak cry
Weak cry 		42 0 1 8.2E-04 0 0