Disease #00640 (CFC1 (cardiofaciocutaneous syndrome, type 1 (CFC-1)), OMIM:115150)

Official abbreviation CFC1
Name cardiofaciocutaneous syndrome, type 1 (CFC-1)
OMIM ID 115150
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 4 genes BRAF, KRAS, MAP2K1, MAP2K2
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

3 entries on 1 page. Showing entries 1 - 3.
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00057915 - - - M ? Netherlands - - - no - CFC1 - - - - 1 Manon van Huijkelom
00206191 - - - - - - - - - - - CFC1 - SOS1 SOS1 1 1 LOVD
00466172 - - - F - Brazil - - - - - CFC1 Intellectual disability, Hydronephrosis - BRAF 1 1 Juliana Mazzeu
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