Cardiomyopathy, Dilated, 1gg; Cmd1gg

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Cardiomyopathy, Dilated, 1gg; Cmd1gg

SDHA

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Cardiomyopathy, Dilated, 1gg; Cmd1gg

Seizures
Cardiomyopathy
Dilated cardiomyopathy
Ventricular hypertrophy
Left ventricular hypertrophy
Left ventricular noncompaction
Decreased activity of mitochondrial complex I
Left ventricular noncompaction cardiomyopathy
Decreased activity of mitochondrial complex II

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Cardiomyopathy, Dilated, 1gg; Cmd1gg Recommended genes panels

Panel Name, Specifity and genes Tested/covered
SDHA Sequence Analysis. By Baylor Miraca Genetics Laboratories (United States). SDHA Specificity 100 % Genes 100 %
SDHA Sequence Analysis (Prenatal Diagnosis). By Baylor Miraca Genetics Laboratories (United States). SDHA Specificity 100 % Genes 100 %
Hereditary Renal Cancer Panel. By Baylor Miraca Genetics Laboratories (United States). SDHA, SDHB, SDHC, SDHD, VHL, WT1, CDKN1C, SDHAF2, FLCN, FH, GPC3, MET, PTEN Specificity 8 % Genes 100 %
Hereditary Paraganglioma/Pheochromocytoma Panel. By Baylor Miraca Genetics Laboratories (United States). SDHA, SDHB, SDHC, SDHD, VHL, SDHAF2, TMEM127, MAX, RET Specificity 12 % Genes 100 %
Hereditary Endocrine Cancer Panel. By Baylor Miraca Genetics Laboratories (United States). SDHA, SDHB, SDHC, SDHD, TP53, VHL, CDC73, SDHAF2, TMEM127, MAX, MEN1, PRKAR1A, PTEN, RET Specificity 8 % Genes 100 %
Comprehensive Hereditary Cancer Panel. By Baylor Miraca Genetics Laboratories (United States). RUNX1, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, STK11, EPCAM, TP53, VHL, WT1, CBL, SUFU, CDC73, CDH1, CDK4, CDKN1C, CDKN2A , (...) View the complete list with 39 more genes Panel complete gene list RUNX1, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, STK11, EPCAM, TP53, VHL, WT1, CBL, SUFU, CDC73, CDH1, CDK4, CDKN1C, CDKN2A, CEBPA, SBDS, BRIP1, SDHAF2, TMEM127, PALB2, FLCN, ENG, FH, GATA2, ALK, GPC3, APC, SMAD4, MAX, MEN1, MET, MLH1, MRE11, MSH2, MSH6, MUTYH, NBN, NF2, ATM, PAX5, PMS1, PMS2, PHOX2B, PRF1, PRKAR1A, BARD1, PTCH1, PTEN, PTPN11, RAD50, RAD51C, RAD51D, RET Specificity 2 % Genes 100 %
Respiratory Chain Deficiency. By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). BCS1L, SCO1, SCO2, SDHA, SDHB, SDHC, SDHD, SURF1, UQCRB, LRPPRC, NDUFAF5, COX4I2, NDUFA13, ATPAF2, NDUFAF1, NUBPL, NDUFA11, NDUFAF4, PDHX, COX10 , (...) View the complete list with 35 more genes Panel complete gene list BCS1L, SCO1, SCO2, SDHA, SDHB, SDHC, SDHD, SURF1, UQCRB, LRPPRC, NDUFAF5, COX4I2, NDUFA13, ATPAF2, NDUFAF1, NUBPL, NDUFA11, NDUFAF4, PDHX, COX10, COX15, COX4I1, COX6B1, COX7A1, TACO1, TTC19, SDHAF2, TMEM70, FOXRED1, NDUFAF2, DLAT, FASTKD2, UQCRQ, NDUFAF3, SDHAF1, NDUFA1, NDUFA10, NDUFA2, NDUFA7, NDUFA8, NDUFB6, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS5, NDUFS6, NDUFS7, NDUFS8, NDUFV1, NDUFV3, ATP5F1E, PDHA1, PDHB, PDP1 Specificity 2 % Genes 100 %
Comprehensive Hereditary Cancer Panel. By Genetic Services Laboratory University of Chicago (United States). RUNX1, BLM, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, SRP72, STK11, EPCAM, TERC, TERT, TP53, VHL, IKZF1, SAMD9, SAMD9L, CBL , (...) View the complete list with 33 more genes Panel complete gene list RUNX1, BLM, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, SRP72, STK11, EPCAM, TERC, TERT, TP53, VHL, IKZF1, SAMD9, SAMD9L, CBL, RTEL1, CDH1, CDK4, CDKN2A, CEBPA, DDX41, BRIP1, SDHAF2, TMEM127, PALB2, ANKRD26, ETV6, FH, GATA2, APC, SMAD4, MAX, MEN1, MLH1, MSH2, MSH6, MUTYH, NBN, NF1, ATM, PAX5, PMS2, POLD1, POLE, BAP1, PTEN, PTPN11, RET Specificity 2 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

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