Disease #05978 (CCHS (hypoventilation, central, syndrome, congenital, type 1 (CCHS)))

Official abbreviation CCHS
Name hypoventilation, central, syndrome, congenital, type 1 (CCHS)
OMIM ID -
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene LBX1
Associated tissues -
Disease features -
Remarks -
Date created 2021-10-18 22:33:56 +02:00 (CEST)
Date last edited N/A


Individuals

1 entry on 1 page. Showing entry 1.
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00385931 family PubMed: Hernandez-Miranda 2018 5-generation family, 2 affected brothers, unaffected heterozygous carrier parents/relatives M yes - - - - - - CCHS - LBX1 LBX1 1 1 Johan den Dunnen
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