Disease #01244 (KFS1 (Klippel-Feil syndrome, type 1, autosomal dominant (KFS1)), OMIM:118100)

Official abbreviation KFS1
Name Klippel-Feil syndrome, type 1, autosomal dominant (KFS1)
OMIM ID 118100
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GDF6
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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00382091 208 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - KFS1 microphthalmia, anophthalmia, and coloboma; MIM, 118100 GDF6 GDF6 1 1 LOVD
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