Pages that link to "Template:OMIM"
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The following pages link to Template:OMIM:
Displayed 50 items.
- Rothmund-Thomson syndrome (transclusion) (← links)
- SLC25A10 (transclusion) (← links)
- Brunner syndrome (transclusion) (← links)
- Potassium cyanide (transclusion) (← links)
- Cytochrome b5 (transclusion) (← links)
- Freckles (transclusion) (← links)
- Carnosinemia (transclusion) (← links)
- Jansky-Bielschowsky disease (transclusion) (← links)
- CD79A (transclusion) (← links)
- Gunther disease (transclusion) (← links)
- Argininemia (transclusion) (← links)
- Acrocephalosyndactylia (transclusion) (← links)
- Hyper-IgM syndrome type 2 (transclusion) (← links)
- Hyper-IgM syndrome type 5 (transclusion) (← links)
- Beta amyloid (transclusion) (← links)
- LAMP2 (transclusion) (← links)
- Timeline of tuberous sclerosis (transclusion) (← links)
- Beta-mannosidosis (transclusion) (← links)
- Fibrochondrogenesis (transclusion) (← links)
- Hexokinase deficiency (transclusion) (← links)
- HK1 (transclusion) (← links)
- Acrocallosal syndrome (transclusion) (← links)
- Ichthyosis bullosa of Siemens (transclusion) (← links)
- Hypoplastic left heart syndrome causes (transclusion) (← links)
- Hereditary nonpolyposis colorectal cancer pathophysiology (transclusion) (← links)
- Geroderma osteodysplastica (transclusion) (← links)
- Aplasia cutis congenita (transclusion) (← links)
- Lawrence-Moon syndrome (transclusion) (← links)
- Achalasia-addisonian syndrome (transclusion) (← links)
- Galactose epimerase deficiency (transclusion) (← links)
- Arthrogryposis classification (transclusion) (← links)
- Gaucher's disease pathophysiology (transclusion) (← links)
- Ataxia telangiectasia pathophysiology (transclusion) (← links)
- Thalassemia pathophysiology (transclusion) (← links)
- Maturity onset diabetes of the young pathophysiology (transclusion) (← links)
- Nephrogenic diabetes insipidus causes (transclusion) (← links)
- Papillorenal syndrome overview (transclusion) (← links)
- Potter syndrome classification (transclusion) (← links)
- Retinitis causes (transclusion) (← links)
- Dyskeratosis congenita overview (transclusion) (← links)
- Buschke–Ollendorff syndrome (transclusion) (← links)
- Schindler disease (transclusion) (← links)
- 2-methylbutyryl-coenzyme a dehydrogenase deficiency (transclusion) (← links)
- Hypertryptophanemia (transclusion) (← links)
- WARG syndrome (transclusion) (← links)
- Basement membrane corneal dystrophy (transclusion) (← links)
- Pontocerebellar hypoplasia (transclusion) (← links)
- Permanent neonatal diabetes mellitus (transclusion) (← links)
- Microvillus inclusion disease (transclusion) (← links)
- Transthyretin-related hereditary amyloidosis (transclusion) (← links)