Pages that link to "Template:OMIM2"
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The following pages link to Template:OMIM2:
Displayed 100 items.
- Osteopetrosis (transclusion) (← links)
- Tyrosinemia (transclusion) (← links)
- Cystinuria (transclusion) (← links)
- Brachydactyly (transclusion) (← links)
- Kallman syndrome (transclusion) (← links)
- Arthrogryposis (transclusion) (← links)
- Ehlers-Danlos syndrome (transclusion) (← links)
- Charcot-Marie-Tooth Syndrome (transclusion) (← links)
- Androgen insensitivity syndrome (transclusion) (← links)
- Achondrogenesis (transclusion) (← links)
- Adrenoleukodystrophy (transclusion) (← links)
- Stickler syndrome (transclusion) (← links)
- Epidermolysis bullosa simplex (transclusion) (← links)
- Lesch-Nyhan's syndrome (transclusion) (← links)
- Congenital insensitivity to pain (transclusion) (← links)
- Larsen syndrome (transclusion) (← links)
- Epidermodysplasia verruciformis (transclusion) (← links)
- Achromatopsia (transclusion) (← links)
- Aniridia (transclusion) (← links)
- Vitelliform macular dystrophy (transclusion) (← links)
- X-linked congenital stationary night blindness (transclusion) (← links)
- Retinitis pigmentosa (transclusion) (← links)
- Bare lymphocyte syndrome (transclusion) (← links)
- Bipolar disorder (transclusion) (← links)
- Lissencephaly (transclusion) (← links)
- Nesidioblastosis (transclusion) (← links)
- Autoimmune polyendocrine syndrome (transclusion) (← links)
- Duane syndrome (transclusion) (← links)
- Acute fatty liver of pregnancy (transclusion) (← links)
- Iron overload disorder (transclusion) (← links)
- Uniparental disomy (transclusion) (← links)
- Imperforate anus (transclusion) (← links)
- 3-Methylglutaconic aciduria (transclusion) (← links)
- 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (transclusion) (← links)
- Autosomal dominant nocturnal frontal lobe epilepsy (transclusion) (← links)
- Bartter syndrome (transclusion) (← links)
- Benign familial neonatal convulsions (transclusion) (← links)
- Citrullinemia (transclusion) (← links)
- Congenital disorder of glycosylation (transclusion) (← links)
- Emery-Dreifuss muscular dystrophy (transclusion) (← links)
- Facioscapulohumeral muscular dystrophy (transclusion) (← links)
- Familial atrial fibrillation (transclusion) (← links)
- Familial hemiplegic migraine (transclusion) (← links)
- Generalized epilepsy with febrile seizures plus (transclusion) (← links)
- Hereditary multiple exostoses (transclusion) (← links)
- Hyper-IgE syndrome (transclusion) (← links)
- Juvenile myoclonic epilepsy (transclusion) (← links)
- Kallmann syndrome (transclusion) (← links)
- Muscular dystrophy (transclusion) (← links)
- Myotonic dystrophy (transclusion) (← links)
- Nemaline myopathy (transclusion) (← links)
- Primary ciliary dyskinesia (transclusion) (← links)
- Sanfilippo syndrome (transclusion) (← links)
- Spinocerebellar ataxia (transclusion) (← links)
- Tay-Sachs disease (transclusion) (← links)
- Thyroid hormone resistance (transclusion) (← links)
- Usher syndrome (transclusion) (← links)
- Waardenburg syndrome (transclusion) (← links)
- XX gonadal dysgenesis (transclusion) (← links)
- Xanthinuria (transclusion) (← links)
- Xeroderma pigmentosum (transclusion) (← links)
- Malignant hyperthermia (transclusion) (← links)
- Hereditary stomatocytosis (transclusion) (← links)
- Griscelli syndrome (transclusion) (← links)
- Hypodontia (transclusion) (← links)
- Troponin C (transclusion) (← links)
- Troponin T (transclusion) (← links)
- Troponin I (transclusion) (← links)
- Transglutaminase (transclusion) (← links)
- Cystic medial necrosis (transclusion) (← links)
- GM2 gangliosidoses (transclusion) (← links)
- Intestinal atresia (transclusion) (← links)
- Klippel-Feil syndrome (transclusion) (← links)
- Woolly hair syndrome (transclusion) (← links)
- Congenital nephrotic syndrome (transclusion) (← links)
- Ectrodactyly-ectodermal dysplasia-cleft syndrome (transclusion) (← links)
- Factor XIII deficiency (transclusion) (← links)
- Short rib-polydactyly syndrome (transclusion) (← links)
- Hemophagocytic lymphohistiocytosis (transclusion) (← links)
- Limb-girdle muscular dystrophy (transclusion) (← links)
- Morquio's syndrome (transclusion) (← links)
- Olivopontocerebellar atrophy (transclusion) (← links)
- Distal muscular dystrophy (transclusion) (← links)
- Rhizomelic chondrodysplasia punctata (transclusion) (← links)
- Laron syndrome (transclusion) (← links)
- Complement deficiency (transclusion) (← links)
- Epidermolysis bullosa dystrophica (transclusion) (← links)
- Senior-Løken syndrome (transclusion) (← links)
- Essential tremor (transclusion) (← links)
- G-protein coupled receptor kinases (transclusion) (← links)
- Transglutamination (transclusion) (← links)
- Hypogammaglobulinemia (transclusion) (← links)
- Autoimmune lymphoproliferative syndrome (transclusion) (← links)
- Camurati-Engelmann disease (transclusion) (← links)
- Hereditary motor and sensory neuropathy (transclusion) (← links)
- Lesch-Nyhan syndrome (transclusion) (← links)
- Hawkinsinuria (transclusion) (← links)
- 2-Hydroxyglutaric aciduria (transclusion) (← links)
- Hereditary sensory and autonomic neuropathy (transclusion) (← links)
- Chronic mucocutaneous candidiasis (transclusion) (← links)