Assessment of Indian Economy During Covid-19

Last uploaded: July 5, 2021

Id	http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000003536 http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000003536
Preferred Name	Porphyria, Acute Intermittent [Disease/Finding]
Type	http://www.w3.org/2002/07/owl#Class

label	Porphyria, Acute Intermittent [Disease/Finding]
prefLabel	Porphyria, Acute Intermittent [Disease/Finding]
SNOMED_CID	234422006
NUI	N0000003536
Synonym	Acute Porphyria
code	C7250
prefixIRI	NDF-RT:N0000003536
RxNorm_CUI	1023116
subClassOf	http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000003528
imported from	http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl
MeSH_CUI	M0026010
MeSH_DUI	D017118
type	http://www.w3.org/2002/07/owl#NamedIndividual http://www.w3.org/2002/07/owl#Class
MeSH_Name	Porphyria, Acute Intermittent
UMLS_CUI	C0162565
Display_Name	Porphyria, Acute Intermittent
MeSH_Definition	An autosomal dominant porphyria that is due to a deficiency of HYDROXYMETHYLBILANE SYNTHASE in the LIVER, the third enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features are recurrent and life-threatening neurologic disturbances, ABDOMINAL PAIN, and elevated level of AMINOLEVULINIC ACID and PORPHOBILINOGEN in the urine.

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