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Differential Diagnosis For Family history/Parental consanguinity
List of current finding(s):
Family history/Parental consanguinity
- Metabolic, Storage Disorders
- Xanthinuria
- Phenylketonuria/PKU
- Wilsons Disease
- Alkaptonuria/Ochronosis
- Aspartylglycosaminuria
- Fructosuria, essential
- Galactosemia
- Hartnup disease
- Juvenile ceroid lipofuscinosis/Batten-M
- Tryptophanemia
- 5 alpha Reductase Deficiency Syndrome
- Congenital, Developmental Disorders
- Mental retardation
- Hereditary, Familial, Genetic Disorders
- Thalassemia major
- Alpha 1 antitrypsin deficiency
- Cystic fibrosis (mucoviscidosis)
- Lipodystrophy/familial/dominant
- Gittleman's syndrome
- Dominant SCA/Spinal Cerebellar ataxias
- Bartter's syndrome
- Friedreich's Ataxia
- Laurence-Moon-Biedel syndrome
- Leprechaunism
- Lipodystrophy, generalized
- Muscular atrophy, infantile, spinal
- Pallidopyramidal hereditary syndrome
- Sjogren-Larsson syndrome
- Usage, Degenerative, Necrosis, Age Related Disorders
- Metachromatic leukodystrophy
- Eponymic, Esoteric Disorders
- Usher's syndrome
- Synonyms
- Consanguinities, consanguinity, Consanguinity (finding), History, parent, Parent (person), Parent of, Parent of (observable entity), Parental, Parents
- External Links Related to Family history/Parental consanguinity
- Wikipedia
- Merck
- Images
- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)
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© 2013 MedTech USA, Inc. (last modified on 05/19/13)
