Disease #00605 (FRASRS1 (Fraser syndrome), OMIM:219000)

Official abbreviation FRASRS1
Name Fraser syndrome
OMIM ID 219000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 3 genes FRAS1, FREM2, GRIP1
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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00095117 - - - ? no - - - - Yes - FRASRS1 Bilateral renal agenesis - FRAS1 2 1 Karen Stals
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