Pages that link to "Autosomal dominant"
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The following pages link to Autosomal dominant:
Displayed 50 items.
- Greig cephalopolysyndactyly syndrome (← links)
- Hay-Wells syndrome (← links)
- Hereditary multiple exostoses (← links)
- Holt-Oram syndrome (← links)
- Hyper-IgE syndrome (← links)
- Hyperkalemic periodic paralysis (← links)
- Hypermethioninemia (← links)
- Hypochondrogenesis (← links)
- Hypochondroplasia (← links)
- Hypokalemic periodic paralysis (← links)
- Infantile cortical hyperostosis (← links)
- Jackson-Weiss syndrome (← links)
- Kniest dysplasia (← links)
- Li-Fraumeni syndrome (← links)
- Liddle's syndrome (← links)
- Metachondromatosis (← links)
- Muscular dystrophy (← links)
- Myotonia congenita (← links)
- Myotonic dystrophy (← links)
- Nemaline myopathy (← links)
- Neurofibromatosis type II (← links)
- Nevoid basal cell carcinoma syndrome (← links)
- Pachyonychia congenita (← links)
- Pallister-Hall syndrome (← links)
- Paramyotonia congenita (← links)
- Periodic paralysis (← links)
- Photic sneeze reflex (← links)
- Platyspondylic lethal skeletal dysplasia, Torrance type (← links)
- Potassium-aggravated myotonia (← links)
- Rubinstein-Taybi syndrome (← links)
- SADDAN (← links)
- Snatiation (← links)
- Spinocerebellar ataxia (← links)
- Spinocerebellar ataxia type-13 (← links)
- Spinocerebellar ataxia type-6 (← links)
- Spondyloepimetaphyseal dysplasia, Strudwick type (← links)
- Spondyloepiphyseal dysplasia congenita (← links)
- Tangier disease (← links)
- Timothy syndrome (← links)
- Townes-Brocks syndrome (← links)
- Variegate porphyria (← links)
- WHIM syndrome (← links)
- Waardenburg syndrome (← links)
- Malignant hyperthermia (← links)
- List of genetic engineering topics (← links)
- Presenilin (← links)
- CTLA-4 (← links)
- MSH2 (← links)
- Huntingtin (← links)
- Fibroblast growth factor receptor 1 (← links)