Acetylation, Slow

Clinical Features

Phenotypes and symptoms related to Acetylation, Slow

  • Neoplasm
  • Peripheral neuropathy
  • Abnormality of metabolism/homeostasis
  • Systemic lupus erythematosus
  • Bladder neoplasm

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.

Alternative names

Acetylation, Slow Is also known as inh inactivation, slow, isoniazid inactivation, slow, slow acetylator phenotype.

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.


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Acetylation, Slow Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Pharmacogenetics (NAT2 polymorphisms).

By CGC Genetics (Portugal).

NAT2
Specificity
100 %
Genes
100 %
Slow Acetylation, Drug-Induced Hepatotoxicity, and Other Adverse Drug Reactions via NAT2 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

NAT2
Specificity
100 %
Genes
100 %
Pharmacogenetic panel.

By bio.logis Center for Human Genetics Diagnosticum (Germany).

SLC19A1, SLCO1B1, SOD2, TPMT, UGT1A1, CCR5, VKORC1, ADH1B, CYP2B6, CYP2C19, CYP2C9, CYP2D6, CYP3A4, CYP3A5, ADRB3, DPYD, ABCB1, G6PD, MTHFR, NAT2 , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
100 %
NAT2.

By MVZ Dortmund Dr. Eberhard & Partner (Germany).

NAT2
Specificity
100 %
Genes
100 %
NAT2 (N-Acetylransferase): *5A, *6A, and *7A alleles screening.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases (Spain).

NAT2
Specificity
100 %
Genes
100 %
NAT2.

By Fulgent Genetics Fulgent Genetics (United States).

NAT2
Specificity
100 %
Genes
100 %
NAT2.

By Genelex (United States).

NAT2
Specificity
100 %
Genes
100 %
Slow acetylator due to N-acetyltransferase enzyme variant.

By Labor Dr. Wisplinghoff (Germany).

NAT2
Specificity
100 %
Genes
100 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like WEILL-MARCHESANI SYNDROME 3; WMS3 MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS9 HYPOKALEMIC PERIODIC PARALYSIS GENETIC TRANSIENT CONGENITAL HYPOTHYROIDISM AICARDI-GOUTIERES SYNDROME 3; AGS3 AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1 BLEEDING DISORDER, PLATELET-TYPE, 11; BDPLT11

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