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Differential Diagnosis For Short stature: Hereditary, Familial, Genetic Disorders

List of current finding(s):

Hereditary, Familial, Genetic Disorders: next: Degenerative-Age Related Causes: Hereditary disorder; Hereditary renal disease; Granulomatous dis/childhood, chronic; Osteopetrosis (Albers-Schonberg); Thalassemia major; Agammaglobulinemia, x-linked, infantile; Pyruvate kinase deficiency RBC's; Sickle cell anemia; Achondrogenesis I/Parenti-Fraccaro; Cleidocranial digital dysostosis; Cystic fibrosis (mucoviscidosis); Nephritis, hereditary (Alports); Neurofibromatosis; Osteogenesis imperfecta; Pseudo-pseudohypoparathyroidism; Jarcho-Levin Spondylocostal dysplasia Syndrome; Johanson Blizzard genetic syndrome (unco); Juberg Marsidi Genetic syndrome (unco); Marinesco Sjogren syndrome; Mitochondrial myopathy/MERRF; Myhre Syndrome; Pitt syndrome (4p16.3); MELAS Encephalopathy; Pseudohypoparathyroidism; Weill-Marchesani syndrome; Zellweger Cerebrhepatorenal syndrome; Achondrogenesis II/Langer-Saldino; Acrocephalosyndactyly type III syndrome; Bartter's syndrome; Bird-headed dwarf of Seckel; Borjeson-Forssman-Lehmann Syn/BFLS (xq26.3); Chondrodysplasia punctata/calcificans (Conradi); Cockayne syndrome; Dolichospondylic dysplasia; Dysautonomia, familial; Fanconi's pancytopenia-dysmelia synd; Hyperphosphatasia, hereditary; Hypophosphatemia, familial; Kearns-Sayre Ophthalmoplegic Syndrome; Leprechaunism; Maffucci syndrome; Metaphyseal chondrodysplasia; Oculocerebrorenal dystrophy/Lowe syndrome; Osteodysplasia, familial (Melnick Needles); Schwartz-Jampel syndrome; Scott's Craniodigital syndrome; SHORT syndrome (Rieger anomaly plus); Shwachman (Shwachman-Diamond) syndrome; Sjogren-Larsson syndrome; Smith-Lemli-Opitz syndrome; Spondylometaphyseal dysplasia syndrome; Thalassemia-hemoglobin C disease; Williams syndrome/Elfin facies; Winchester syndrome; Brooks syndrome; Chromosome 20 deletion/Ring syndrome; Chudley Syndrome 1; Curran acrorenal syndrome; Familial testotoxicosis/Premature puberty [2p21]; Familial Vitamin D dependent Rickets; Kabuki make-up syndrome; MASA Syndrome; Multiple Hereditary Exostosis; Reiger Syndrome; Say Syndrome 1; Segawa Syndrome/Infant Parkinsonism

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