Disease Browser
Parent Node: Diabetic Angiopathies (D003925) ..Starting node .. MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (OMIM:612635) Child Nodes:
Sister Nodes: ..Diabetic Foot (D017719) ..Diabetic Retinopathy (D003930) 1 ..MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1 (OMIM:603933) ..MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 2 (OMIM:612623) ..MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 3 (OMIM:612624) ..MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4 (OMIM:612628) ..MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (OMIM:612633) ..MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 (OMIM:612634) ..MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (OMIM:612635) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 7267
Name: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7
Definition:
Alternative IDs:
ParentIDs: MESH:D003925
TreeNumbers: C14.907.320/612635 |C19.246.099.500/612635
Synonyms: MVCD7 |NEPHROPATHY, DIABETIC, SUSCEPTIBILITY TO |NONPROLIFERATIVE RETINOPATHY, DIABETIC, SUSCEPTIBILITY TO |PROLIFERATIVE RETINOPATHY, DIABETIC, SUSCEPTIBILITY TO
Slim Mappings: Cardiovascular disease|Endocrine system disease
Reference:
MedGen: 612635
MeSH: 612635
OMIM: 612635 ; Genes: HFE ; Phenotypes Disease Causing ClinVar Variants Variation_Name GeneID GeneSymbol ClinicalSignificance dbSNP RCVaccession TestedInGTR PhenotypeIDs Chromosome Start Stop HGVS_c HGVS_p HGVS_g OtherIDs Disease_ClinVar Disease_hgmd NM_000410.3(HFE):c.187C>G (p.His63Asp) 3077 HFE Likely benign;Pathogenic;risk factor 1799945 RCV000000026 ; RCV000000027 ; RCV000175607 ; RCV000117220 ; Y MedGen:C0392514,OMIM:235200; MedGen:C2673520,OMIM:612635; MedGen:CN169374; MedGen:CN221809 6 26091179 26091179 NM_000410.3:c.187C>G NP_000401.1:p.His63Asp NC_000006.11:g.26091179C>G OMIM Allelic Variant:613609.0002 C0392514 235200 Hemochromatosis type 1; C2673520 612635 Microvascular complications of diabetes 7; CN221809 not provided; CN169374 not specified NM_000410.3(HFE):c.845G>A (p.Cys282Tyr) 3077 HFE Benign;Pathogenic;association;risk factor 1800562 RCV000000019 ; RCV000000020 ; RCV000000021 ; RCV000000022 ; RCV000000023 ; RCV000000024 ; RCV000000025 ; RCV000178096 ; RCV000117222 ; RCV000210820 ; Y ; MedGen:C0027672,SNOMED CT:699346009; MedGen:C0392514,OMIM:235200; MedGen:C2673520,OMIM:612635; MedGen:C3150862; MedGen:C3280096,OMIM:614193; MedGen:CN169374; MedGen:CN221809 6 26093141 26093141 NM_000410.3:c.845G>A NP_000401.1:p.Cys282Tyr NC_000006.11:g.26093141G>A OMIM Allelic Variant:613609.0001 C0392514 235200 Hemochromatosis type 1; C3150862 Hemochromatosis, juvenile, digenic; C0027672 Hereditary cancer-predisposing syndrome; C2673520 612635 Microvascular complications of diabetes 7; CN221809 not provided; CN169374 not specified; C3280096