(Q4751018)

English

Analbuminaemia

Congenital analbuminemia (CAA) is characterized by the absence or dramatic reduction of circulating human serum albumin (HSA)

Analbuminemia
ANALBA
ANALBUMINEMIA; ANALBA

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genetic hematologic disease

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

2 references

13 August 2019

Splicing mutation in human hereditary analbuminemia

NCI Thesaurus ID

C124851

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exact match

http://www.orpha.net/ORDO/Orphanet_86816

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Identifiers

GARD rare disease ID

13056

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

Microsoft Academic ID

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mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

imported from Wikimedia project

English Wikipedia

Wikimedia import URL

https://en.wikipedia.org/w/index.php?title=Analbuminaemia&oldid=948417879

UMLS CUI

C0878666

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

(Q4751018)

Analbuminaemia

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