Genomics England
GMS Panels
Panels
Genes and Entities
CLMP
CXADR like membrane protein
OMIM:
611693
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Panel
Mode of inheritance
Details
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in
Intestinal failure or congenital diarrhoea
R-numbers:
R331
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Congenital short bowel syndrome, OMIM:615237