The following pages link to Antley–Bixler syndrome
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Genetic disorder (links | edit)
- Tutankhamun (links | edit)
- 5α-Reductase 2 deficiency (links | edit)
- Achondroplasia (links | edit)
- Akhenaten (links | edit)
- Cenani–Lenz syndactylism (links | edit)
- List of diseases (A) (links | edit)
- Hirschsprung's disease (links | edit)
- Congenital hypothyroidism (links | edit)
- Congenital adrenal hyperplasia (links | edit)
- Osteosclerosis (links | edit)
- Osteopetrosis (links | edit)
- Gastrointestinal stromal tumor (links | edit)
- Waardenburg syndrome (links | edit)
- Lipoid congenital adrenal hyperplasia (links | edit)
- Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency (links | edit)
- Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency (links | edit)
- Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency (links | edit)
- Hereditary hemorrhagic telangiectasia (links | edit)
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (links | edit)
- Glanzmann's thrombasthenia (links | edit)
- Osteogenesis imperfecta (links | edit)
- Persistent Müllerian duct syndrome (links | edit)
- Hereditary multiple exostoses (links | edit)
- Kallmann syndrome (links | edit)
- Congenital insensitivity to pain with anhidrosis (links | edit)
- Inborn errors of metabolism (links | edit)
- Crouzon syndrome (links | edit)
- Ellis–Van Creveld syndrome (links | edit)
- Aspirin-exacerbated respiratory disease (links | edit)
- Diastrophic dysplasia (links | edit)
- Atelosteogenesis, type II (links | edit)
- Apert syndrome (links | edit)
- Fibrous dysplasia of bone (links | edit)
- Thanatophoric dysplasia (links | edit)
- X-linked ichthyosis (links | edit)
- Achondrogenesis (links | edit)
- Smith–Lemli–Opitz syndrome (links | edit)
- 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency (links | edit)
- Enchondroma (links | edit)
- Osteodystrophy (links | edit)
- Osteochondroma (links | edit)
- Hypochondrogenesis (links | edit)
- Achondrogenesis type 2 (links | edit)
- Otospondylomegaepiphyseal dysplasia (links | edit)
- Spondyloepiphyseal dysplasia congenita (links | edit)
- Leber congenital amaurosis (links | edit)
- Hypogammaglobulinemia (links | edit)
- Hypochondroplasia (links | edit)
- Common variable immunodeficiency (links | edit)