Musculoskeletal Diseases | Page 1

645 diseases found in 7 pages

1 Diseases

12q14 microdeletion syndrome

2 Diseases

2q37 deletion syndrome

3 Diseases

3M syndrome

A Diseases

Absence of Tibia Absence of tibia with polydactyly Absent patella Acheiropody Achondrogenesis type 1A Achondrogenesis type 1B Achondrogenesis type 2 Achondroplasia Acrocallosal syndrome, Schinzel type Acrocapitofemoral dysplasia Acrocephalopolydactyly Acrodysostosis Acrodysplasia scoliosis Acrofacial dysostosis Catania type Acrofacial dysostosis Palagonia type Acrofacial dysostosis Rodriguez type Acrofrontofacionasal dysostosis syndrome Acromelic frontonasal dysostosis Acromesomelic dysplasia Acromesomelic dysplasia Hunter Thompson type Acromesomelic dysplasia Maroteaux type Acromicric dysplasia Acroosteolysis dominant type Acropectoral syndrome Acro-pectoro-renal field defect Acropectorovertebral dysplasia F form Acute febrile neutrophilic dermatosis Adactylia unilateral Adams-Oliver syndrome Adenosine Deaminase 2 deficiency Adult-onset Still's disease ADULT syndrome Aicardi-Goutieres syndrome Al Gazali Sabrinathan Nair syndrome Allain-Babin-Demarquez syndrome Alpha-mannosidosis Amyotrophy, neurogenic scapuloperoneal, New England type Anauxetic dysplasia Angel shaped phalangoepiphyseal dysplasia Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Ankylosing spondylitis Ankylosing vertebral hyperostosis with tylosis Anonychia-onychodystrophy with hypoplasia or absence of distal phalanges Antley Bixler syndrome Apert syndrome Arthrogryposis multiplex congenita Arts syndrome Aspartylglycosaminuria Atelosteogenesis type 1 Atelosteogenesis type 2 Atelosteogenesis type 3 Auralcephalosyndactyly Auriculo-condylar syndrome Auriculoosteodysplasia Autosomal dominant spondyloepiphyseal dysplasia tarda Autosomal recessive early-onset inflammatory bowel disease Autosomal recessive protein C deficiency Axial osteomalacia Axial spondylometaphyseal dysplasia

B Diseases

Baby rattle pelvic dysplasia Baller-Gerold syndrome Banki syndrome Beare-Stevenson cutis gyrata syndrome Behçet disease Benallegue Lacete syndrome Bethlem myopathy Beukes familial hip dysplasia Blau syndrome Blount disease BOD syndrome Bone dysplasia Azouz type Bone dysplasia lethal Holmgren type Boomerang dysplasia Bowing of legs, anterior with dwarfism Brachycephalofrontonasal dysplasia Brachydactylous dwarfism Mseleni type Brachydactyly elbow wrist dysplasia Brachydactyly long thumb type Brachydactyly Mononen type Brachydactyly type A1 Brachydactyly type A2 Brachydactyly type A4 Brachydactyly type A5 Brachydactyly type A6 Brachydactyly type A7 Brachydactyly type B Brachydactyly type C Brachydactyly type E Brachydactyly types B and E combined Brachyolmia type 3 Branchial arch syndrome X-linked Brody myopathy Bruck syndrome 1 Buschke Ollendorff syndrome

C Diseases

Caffey disease Campomelia Cumming type Campomelic dysplasia

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

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