Disease #01704 (KFS2 (Klippel-Feil syndrome, type 2, autosomal recessive (KFS-2)), OMIM:214300)

Official abbreviation KFS2
Name Klippel-Feil syndrome, type 2, autosomal recessive (KFS-2)
OMIM ID 214300
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene MEOX1
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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00229762 - - - F yes Saudi Arabia Arab - - - - KFS2 - MEOX1 MEOX1 1 1 Fowzan Alkuraya
00229763 - - - M yes Saudi Arabia Arab - - - - KFS2 - MEOX1 MEOX1 1 1 Fowzan Alkuraya
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