Disease #03338 (FND3 (dysplasia, frontonasal, type 3), OMIM:613456)

Official abbreviation FND3
Name dysplasia, frontonasal, type 3
OMIM ID 613456
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene ALX1
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

2 entries on 1 page. Showing entries 1 - 2.
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00204588 - - - - yes Turkey - - - - - FND3 - ALX1 ALX1 1 1 LOVD
00204589 - - parents distantly related - - Turkey - - - - - FND3 - ALX1 ALX1 1 1 LOVD
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