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searching for Propionic acidemia 10 found (41 total)

alternate case: propionic acidemia

Multiple carboxylase deficiency (121 words) [view diff] no match in snippet view article find links to article

Multiple carboxylase deficiency is a form of metabolic disorder involving failures of carboxylation enzymes. The deficiency can be in biotinidase or holocarboxylase
Methylmalonic acid (1,215 words) [view diff] exact match in snippet view article find links to article
guidelines for the diagnosis and management of methylmalonic and propionic acidemia". Orphanet Journal of Rare Diseases. 9 (1): 130. doi:10.1186/s13023-014-0130-8
Pancytopenia (794 words) [view diff] case mismatch in snippet view article find links to article
anemia Medication Hypersplenism Osteopetrosis Organic acidurias (Propionic Acidemia, Methylmalonic Aciduria, Isovaleric Aciduria) Low dose arsenic poisoning
Anaplerotic reactions (606 words) [view diff] exact match in snippet view article find links to article
guidelines for the diagnosis and management of methylmalonic and propionic acidemia". Orphanet Journal of Rare Diseases. 9 (1): 130. doi:10.1186/s13023-014-0130-8
Methylmalonyl-CoA (603 words) [view diff] exact match in snippet view article find links to article
guidelines for the diagnosis and management of methylmalonic and propionic acidemia". Orphanet Journal of Rare Diseases. 9 (1): 130. doi:10.1186/s13023-014-0130-8
Metab-L (827 words) [view diff] exact match in snippet view article find links to article
"Clinical, pathological, and biochemical studies in a patient with propionic acidemia and fatal cardiomyopathy" (PDF). Molecular Genetics and Metabolism
List of genetic disorders (995 words) [view diff] exact match in snippet view article find links to article
1-3:1,000,000 Patau syndrome (Trisomy 13) 13 trisomy PCC deficiency (propionic acidemia) PC recessive 1:250,000 Porphyria cutanea tarda (PCT) UROD dominant
List of diseases (M) (2,469 words) [view diff] exact match in snippet view article
carboxylase deficiency, late onset Multiple carboxylase deficiency, propionic acidemia Multiple chemical sensitivity Multiple congenital anomalies mental
Heritability of autism (10,913 words) [view diff] exact match in snippet view article find links to article
disorders like fragile X syndrome; metabolic conditions (for example, propionic acidemia); and chromosomal disorders like 22q13 deletion syndrome and 16p11
Anti-ulcer agents (3,318 words) [view diff] exact match in snippet view article find links to article
Deodato F, et al. (September 2018). "Axonal peripheral neuropathy in propionic acidemia: A severe side effect of long-term metronidazole therapy". Neurology