Disease #03396 (KFS3 (Klippel-Feil syndrome, type 3, autosomal dominant (KFS-3)), OMIM:613702)

Official abbreviation KFS3
Name Klippel-Feil syndrome, type 3, autosomal dominant (KFS-3)
OMIM ID 613702
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GDF3
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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00382090 190 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - KFS3 microphthalmia, anophthalmia, and coloboma; MIM, 613702 GDF3 GDF3 1 1 LOVD
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