Misplaced Pages

The following pages link to Template:Cell surface receptor deficiencies

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• transclusion count
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Showing 50 items.

• Charcot–Marie–Tooth disease (links | edit)
• Genetic disorder (transclusion) (links | edit)
• Integrin (links | edit)
• Achondroplasia (transclusion) (links | edit)
• Hereditary haemochromatosis (links | edit)
• Cenani–Lenz syndactylism (transclusion) (links | edit)
• Cleft lip and cleft palate (links | edit)
• Hirschsprung's disease (transclusion) (links | edit)
• Congenital hypothyroidism (transclusion) (links | edit)
• Limb–girdle muscular dystrophy (links | edit)
• Osteopetrosis (transclusion) (links | edit)
• Gastrointestinal stromal tumor (transclusion) (links | edit)
• Arrhythmogenic cardiomyopathy (links | edit)
• Waardenburg syndrome (transclusion) (links | edit)
• Hereditary hemorrhagic telangiectasia (transclusion) (links | edit)
• Glanzmann's thrombasthenia (transclusion) (links | edit)
• Persistent Müllerian duct syndrome (transclusion) (links | edit)
• Kallmann syndrome (transclusion) (links | edit)
• Congenital insensitivity to pain with anhidrosis (transclusion) (links | edit)
• Crouzon syndrome (transclusion) (links | edit)
• Aspirin-exacerbated respiratory disease (transclusion) (links | edit)
• Apert syndrome (transclusion) (links | edit)
• Thanatophoric dysplasia (transclusion) (links | edit)
• Leber congenital amaurosis (transclusion) (links | edit)
• Hypogammaglobulinemia (transclusion) (links | edit)
• Hypochondroplasia (transclusion) (links | edit)
• Common variable immunodeficiency (transclusion) (links | edit)
• ABCD syndrome (transclusion) (links | edit)
• Jackson–Weiss syndrome (transclusion) (links | edit)
• Pfeiffer syndrome (transclusion) (links | edit)
• Nephrogenic diabetes insipidus (transclusion) (links | edit)
• Pseudohypoparathyroidism (transclusion) (links | edit)
• Familial male-limited precocious puberty (transclusion) (links | edit)
• Glycoprotein IIb/IIIa (links | edit)
• X-linked severe combined immunodeficiency (transclusion) (links | edit)
• Selective immunoglobulin A deficiency (transclusion) (links | edit)
• Nevoid basal-cell carcinoma syndrome (transclusion) (links | edit)
• Piebaldism (transclusion) (links | edit)
• Robinow syndrome (transclusion) (links | edit)
• XX gonadal dysgenesis (transclusion) (links | edit)
• Integrin alpha X (links | edit)
• Integrin alpha L (links | edit)
• Dejerine–Sottas disease (links | edit)
• Integrin alpha M (links | edit)
• Distal myopathy (links | edit)
• TNF receptor associated periodic syndrome (transclusion) (links | edit)
• Loeys–Dietz syndrome (transclusion) (links | edit)
• Hypohidrotic ectodermal dysplasia (transclusion) (links | edit)
• Kindler syndrome (links | edit)
• Familial hypercholesterolemia (transclusion) (links | edit)