The following pages link to Jansen's metaphyseal chondrodysplasia
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Genetic disorder (links | edit)
- Achondroplasia (links | edit)
- Cenani–Lenz syndactylism (links | edit)
- Hirschsprung's disease (links | edit)
- Congenital hypothyroidism (links | edit)
- Osteosclerosis (links | edit)
- Osteopetrosis (links | edit)
- Gastrointestinal stromal tumor (links | edit)
- Waardenburg syndrome (links | edit)
- Jansen (links | edit)
- Hereditary hemorrhagic telangiectasia (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)
- 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)
- Achondrogenesis (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)
- ABCD syndrome (links | edit)
- Achondrogenesis type 1B (links | edit)
- Polyostotic fibrous dysplasia (links | edit)
- Chondrodystrophy (links | edit)
- Jackson–Weiss syndrome (links | edit)
- Pfeiffer syndrome (links | edit)
- Nephrogenic diabetes insipidus (links | edit)
- Pseudohypoparathyroidism (links | edit)
- Familial male-limited precocious puberty (links | edit)
- List of ICD-9 codes 740–759: congenital anomalies (links | edit)
- Autosomal recessive multiple epiphyseal dysplasia (links | edit)
- X-linked severe combined immunodeficiency (links | edit)
- Selective immunoglobulin A deficiency (links | edit)