MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0340978
Disease: May-Hegglin anomaly
May-Hegglin anomaly 		1.000 CausalMutation phenotype CLINVAR
CUI: C1854520
Disease: SEBASTIAN SYNDROME
SEBASTIAN SYNDROME 		1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C1854520
Disease: SEBASTIAN SYNDROME
SEBASTIAN SYNDROME 		1.000 CausalMutation disease CLINVAR
CUI: C1854520
Disease: SEBASTIAN SYNDROME
SEBASTIAN SYNDROME 		1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C1854520
Disease: SEBASTIAN SYNDROME
SEBASTIAN SYNDROME 		1.000 GermlineCausalMutation disease ORPHANET
CUI: C1863659
Disease: DEAFNESS, AUTOSOMAL DOMINANT 17
DEAFNESS, AUTOSOMAL DOMINANT 17 		0.710 Biomarker disease GENOMICS_ENGLAND
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.540 GeneticVariation disease UNIPROT
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.490 Biomarker disease HPO
CUI: C0033687
Disease: Proteinuria
Proteinuria 		0.400 Biomarker phenotype HPO
CUI: C4280711
Disease: Leukocyte inclusion bodies
Leukocyte inclusion bodies 		0.400 Biomarker phenotype HPO
CUI: C2931716
Disease: Deafness, autosomal dominant nonsyndromic sensorineural 17
Deafness, autosomal dominant nonsyndromic sensorineural 17 		0.300 Biomarker disease CTD_human
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.200 GeneticVariation group CLINVAR
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		0.200 Biomarker group HPO
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		0.200 Biomarker phenotype HPO
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		0.200 GeneticVariation phenotype CLINVAR
CUI: C0027697
Disease: Nephritis
Nephritis 		0.140 Biomarker disease HPO
CUI: C0272278
Disease: Congenital thrombocytopenia
Congenital thrombocytopenia 		0.120 Biomarker disease HPO
CUI: C0154971
Disease: Presenile cataract
Presenile cataract 		0.110 Biomarker disease HPO
CUI: C0014591
Disease: Epistaxis
Epistaxis 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0014591
Disease: Epistaxis
Epistaxis 		0.100 Biomarker phenotype HPO
CUI: C0018780
Disease: Hearing Loss, High-Frequency
Hearing Loss, High-Frequency 		0.100 Biomarker disease HPO
CUI: C0025323
Disease: Menorrhagia
Menorrhagia 		0.100 Biomarker phenotype HPO
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.100 Biomarker disease HPO
CUI: C0028754
Disease: Obesity
Obesity 		0.100 GeneticVariation disease CLINVAR
CUI: C0151529
Disease: Prolonged bleeding time
Prolonged bleeding time 		0.100 Biomarker phenotype HPO