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

Official abbreviation KFS-2
Name Klippel-Feil syndrome, type 2, autosomal recessive (KFS-2)
OMIM ID 214300
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene MEOX1
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Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00229762 - - - F yes Saudi Arabia Arab - 0 - - KFS-2 - MEOX1 MEOX1 1 1 Fowzan Alkuraya
00229763 - - - M yes Saudi Arabia Arab - 0 - - KFS-2 - MEOX1 MEOX1 1 1 Fowzan Alkuraya
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