Disease #01755 (CSID (sucrase-isomaltase deficiency, congenital (CSID)), OMIM:222900)

Official abbreviation CSID
Name sucrase-isomaltase deficiency, congenital (CSID)
OMIM ID 222900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SI
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00027194 - PubMed: Marcadier 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Canada Inuit - - - - CSID see paper; 5d-decreased alertness, hypotonia, hypothermia, admitted to hospital for hemodynamic and ventilatory support for suspected sepsis; ... SI SI 1 1 Johan den Dunnen
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