Analbuminaemia
Congenital analbuminemia (CAA) is characterized by the absence or dramatic reduction of circulating human serum albumin (HSA)
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Analbuminaemia
Summary
Analbuminaemia is a rare disease[1]. Analbuminaemia draws 1 Wikipedia views per month (rare_disease category, ranking #237 of 627).[2]
Key Facts
- Analbuminaemia's instance of is recorded as rare disease[3].
- Analbuminaemia's instance of is recorded as class of disease[4].
- Analbuminaemia's subclass of is recorded as hypoalbuminemia[5].
- Analbuminaemia's subclass of is recorded as genetic hematologic disease[6].
- Analbuminaemia's OMIM ID is recorded as 616000[7].
- Analbuminaemia's Orphanet ID is recorded as 86816[8].
- Analbuminaemia's NCI Thesaurus ID is recorded as C124851[9].
- Analbuminaemia's health specialty is recorded as endocrinology[10].
- Analbuminaemia's genetic association is recorded as blood albumin[11].
- Analbuminaemia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_86816[12].
- Analbuminaemia's UMLS CUI is recorded as C0878666[13].
- Analbuminaemia's ICD-10-CM is recorded as R77.0[14].
- Analbuminaemia's GARD rare disease ID is recorded as 13056[15].
- Analbuminaemia's Mondo ID is recorded as MONDO_0014449[16].
- Analbuminaemia's SNOMED CT ID is recorded as 129232009[17].
- Analbuminaemia's Microsoft Academic ID is recorded as 2778753376[18].
- Analbuminaemia's ICD-11 ID is recorded as 1710972193[19].
- Analbuminaemia's UniProt disease ID is recorded as DI-04235[20].
Why It Matters
Analbuminaemia draws 1 Wikipedia views per month (rare_disease category, ranking #237 of 627).[2]