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Diseases
Genes (667)
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ATXN3
Spinocerebellar Ataxia Type 3
SLC33A1
Spastic Paraplegia 42, Autosomal Dominant
SMARCD1
Foot Deformity
Hand Deformity
PIGB
Foot Deformity
Hand Deformity
SLC26A5
Deafness, Autosomal Recessive 61
AGGF1
Klippel-Trenaunay-Weber Syndrome
FGFR2
Hallux Varus
Joint Stiffness
Ankylosis
FBN1
Hallux Varus
Joint Stiffness
Genu Recurvatum
Hammer Toe
TRPV4
Foot Deformity
Joint Stiffness
Hammer Toe
Contracture
Coxa Vara
COL1A1
Joint Stiffness
Contracture
Coxa Vara
ADAMTSL2
Joint Stiffness
Contracture
ANTXR2
Joint Stiffness
Contracture
PQBP1
Ankylosis
Contracture
PRG4
Contracture
Coxa Vara
LMNA
Foot Deformity
Joint Stiffness
Ankylosis
Contracture
SH2B1
Chromosome 16p11.2 Deletion Syndrome, 220-Kb
SLC18A2
Foot Deformity
Spinocerebellar Ataxia Type 3
COL2A1
Foot Deformity
Joint Stiffness
Contracture
Coxa Vara
EIF4A3
Hand Deformity
TRIP11
Foot Deformity
Hand Deformity
Genu Recurvatum