Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0432284
Disease: Infantile myofibromatosis
Infantile myofibromatosis 		1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C0432284
Disease: Infantile myofibromatosis
Infantile myofibromatosis 		1.000 Biomarker disease CTD_human
CUI: C0432284
Disease: Infantile myofibromatosis
Infantile myofibromatosis 		1.000 Biomarker disease MGD
CUI: C4551572
Disease: MYOFIBROMATOSIS, INFANTILE, 1
MYOFIBROMATOSIS, INFANTILE, 1 		0.800 Biomarker disease MGD
CUI: C4551572
Disease: MYOFIBROMATOSIS, INFANTILE, 1
MYOFIBROMATOSIS, INFANTILE, 1 		0.800 GeneticVariation disease CLINVAR
CUI: C4225270
Disease: Kosaki overgrowth syndrome
Kosaki overgrowth syndrome 		0.730 CausalMutation disease CLINVAR
CUI: C4225270
Disease: Kosaki overgrowth syndrome
Kosaki overgrowth syndrome 		0.730 Biomarker disease CTD_human
CUI: C0393590
Disease: Fahr's syndrome (disorder)
Fahr's syndrome (disorder) 		0.710 Biomarker disease MGD
CUI: C1866182
Disease: Penttinen-Aula syndrome
Penttinen-Aula syndrome 		0.710 Biomarker disease CTD_human
CUI: C1866182
Disease: Penttinen-Aula syndrome
Penttinen-Aula syndrome 		0.710 CausalMutation disease CLINVAR
CUI: C3554321
Disease: BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4 		0.700 Biomarker disease CTD_human
CUI: C3554321
Disease: BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4 		0.700 GeneticVariation disease CLINVAR
CUI: C3554321
Disease: BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4 		0.700 CausalMutation disease CLINVAR
CUI: C0206648
Disease: Myofibromatosis
Myofibromatosis 		0.500 CausalMutation disease CLINVAR
CUI: C0206648
Disease: Myofibromatosis
Myofibromatosis 		0.500 Biomarker disease HPO
CUI: C0206648
Disease: Myofibromatosis
Myofibromatosis 		0.500 Biomarker disease GENOMICS_ENGLAND
CUI: C0013421
Disease: Dystonia
Dystonia 		0.400 Biomarker phenotype HPO
CUI: C0013421
Disease: Dystonia
Dystonia 		0.400 Biomarker phenotype GENOMICS_ENGLAND
CUI: C1851585
Disease: MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA
MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA 		0.400 Biomarker disease CTD_human
CUI: C1851585
Disease: MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA
MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA 		0.400 Biomarker disease HPO
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		0.300 GeneticVariation disease UNIPROT
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder 		0.300 Biomarker disease MGD
CUI: C3165106
Disease: Infiltrating duct carcinoma of female breast
Infiltrating duct carcinoma of female breast 		0.300 GeneticVariation disease UNIPROT
CUI: C4551624
Disease: Idiopathic basal ganglia calcification 1
Idiopathic basal ganglia calcification 1 		0.300 Biomarker disease CTD_human
CUI: C0014457
Disease: Eosinophilia
Eosinophilia 		0.200 Biomarker disease HPO