Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency

Summary

Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency is a rare disease^[1].

Key Facts

• Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency's instance of is recorded as rare disease^[2].
• Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency's instance of is recorded as class of disease^[3].
• Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency's subclass of is recorded as gluconeogenesis disorder^[4].
• Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency's OMIM ID is recorded as 615751^[5].
• Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency's Orphanet ID is recorded as 401948^[6].
• Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency's genetic association is recorded as CA5A^[7].
• Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_401948^[8].
• Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency's UMLS CUI is recorded as C3810404^[9].
• Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency's UMLS CUI is recorded as C4706871^[10].
• Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency's ICD-10-CM is recorded as E74.8^[11].
• Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency's GARD rare disease ID is recorded as 13201^[12].
• Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency's Mondo ID is recorded as MONDO_0014332^[13].
• Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency's Genetics Home Reference Conditions ID is recorded as carbonic-anhydrase-va-deficiency^[14].
• Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency's UniProt disease ID is recorded as DI-04105^[15].