The following pages link to Hydrops-ectopic calcification-moth-eaten skeletal dysplasia
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Charcot–Marie–Tooth disease (links | edit)
- 5α-Reductase 2 deficiency (links | edit)
- Marfan syndrome (links | edit)
- Long QT syndrome (links | edit)
- Limb–girdle muscular dystrophy (links | edit)
- Hereditary spherocytosis (links | edit)
- Congenital adrenal hyperplasia (links | edit)
- Arrhythmogenic cardiomyopathy (links | edit)
- Hypertrophic cardiomyopathy (links | edit)
- Dilated cardiomyopathy (links | edit)
- Epidermolytic hyperkeratosis (links | edit)
- Lipoid congenital adrenal hyperplasia (links | edit)
- Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency (links | edit)
- Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency (links | edit)
- Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency (links | edit)
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (links | edit)
- Alexander disease (links | edit)
- Usher syndrome (links | edit)
- Gardner's syndrome (links | edit)
- Familial adenomatous polyposis (links | edit)
- Inborn errors of metabolism (links | edit)
- Wiskott–Aldrich syndrome (links | edit)
- Palmoplantar keratoderma (links | edit)
- X-linked ichthyosis (links | edit)
- Nemaline myopathy (links | edit)
- Smith–Lemli–Opitz syndrome (links | edit)
- 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency (links | edit)
- Giant axonal neuropathy (links | edit)
- Hereditary elliptocytosis (links | edit)
- Nonsyndromic deafness (links | edit)
- Hereditary pyropoikilocytosis (links | edit)
- Glucocorticoid deficiency 1 (links | edit)
- Apparent mineralocorticoid excess syndrome (links | edit)
- Tauopathy (links | edit)
- Freeman–Sheldon syndrome (links | edit)
- Larsen syndrome (links | edit)
- Epidermolysis bullosa simplex (links | edit)
- Emery–Dreifuss muscular dystrophy (links | edit)
- Short rib–polydactyly syndrome (links | edit)
- Conradi–Hünermann syndrome (links | edit)
- White sponge nevus (links | edit)
- Mevalonate kinase deficiency (links | edit)
- MASS syndrome (links | edit)
- Naegeli–Franceschetti–Jadassohn syndrome (links | edit)
- Laminopathy (links | edit)
- Monilethrix (links | edit)
- May–Hegglin anomaly (links | edit)
- 17β-Hydroxysteroid dehydrogenase III deficiency (links | edit)
- Congenital contractural arachnodactyly (links | edit)
- Buschke–Ollendorff syndrome (links | edit)