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Histidinemia

A hereditary metabolic disorder characterized by increased levels of HISTIDINE in the blood, urine, and cerebrospinal fluid. It is generally benign, but some individuals may be at increased risk for intellectual disability. It is caused by mutations in the histidine ammonia-lyase (HAL) gene. OMIM: 235800.
Also Known As:
Deficiency in Histidase; HAL Deficiency; Histidase deficiency; Histidine ammonia-lyase deficiency; Hyperhistidinemia
Networked: 62 relevant articles (0 outcomes, 10 trials/studies)

Disease Context: Research Results

Related Diseases

1. Citrullinemia
2. Maple Syrup Urine Disease
3. Hartnup Disease
4. Galactosemias (Galactosemia)
5. Propionic Acidemia

Experts

1. Campos, Aline Guimarães: 2 articles (12/2012 - 05/2012)
2. Dutra-Filho, Carlos Severo: 2 articles (12/2012 - 05/2012)
3. Gemelli, Tanise: 2 articles (12/2012 - 05/2012)
4. Rojas, Denise Bertin: 2 articles (12/2012 - 05/2012)
5. Wannmacher, Clóvis Milton Duval: 2 articles (12/2012 - 05/2012)
6. de Andrade, Rodrigo Binkowski: 2 articles (12/2012 - 05/2012)
7. Gu, Wen: 1 article (07/2020)
8. Li, Yiwei: 1 article (07/2020)
9. Liu, Xin: 1 article (07/2020)
10. Su, Jian: 1 article (07/2020)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Histidinemia:
1. Histidine (L-Histidine)FDA Link
2. Histidine Ammonia-LyaseIBA
3. ZincIBA
4. nitromethaneIBA
5. DiamondIBA
6. Reactive Oxygen Species (Oxygen Radicals)IBA
7. TransferasesIBA
8. Carnitine (L-Carnitine)FDA LinkGeneric
9. imidazolelactic acidIBA
10. Amino AcidsFDA Link

Therapies and Procedures

1. Therapeutics
2. Investigational Therapies (Experimental Therapy)
3. Kidney Transplantation
4. Transplantation
5. Diet Therapy (Therapy, Diet)