Disease #04418 (LCCS7 (contracture syndrome, lethal, congenital, type 7 (LCCS-7)), OMIM:616286)

Official abbreviation LCCS7
Name contracture syndrome, lethal, congenital, type 7 (LCCS-7)
OMIM ID 616286
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 CNTNAP1
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00380793 ? PubMed: Nair 2018 - ? - Lebanon - - - - - LCCS7 Arthrogryposis; failure to thrive (Neurological) - CNTNAP1 1 1 LOVD
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