Disease #03831 (CWS5 (Cowden syndrome, type 5 (CWS-5)), OMIM:615108)

Official abbreviation CWS5
Name Cowden syndrome, type 5 (CWS-5)
OMIM ID 615108
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PIK3CA
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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00455153 - - - M yes Spain - - - - - CWS5 HP:0000750 Delayed speech and language development HP:0001270 Motor delay HP:0001300 Parkinsonism HP:0001250 Seizure NO signs of overgrowth Normal brain MRI - PIK3CA 1 1 Maria Elena García Paya
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