Disease #00941 (CSB (Cockayne syndrome, type B (CSB)), OMIM:133540)

Official abbreviation CSB
Name Cockayne syndrome, type B (CSB)
OMIM ID 133540
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 ERCC6
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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00459488 SYD05 IV:4 - - M yes Pakistan - - - - - CSB - - ERCC6 1 4 Amatul Raqeeb Jawaid
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