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Browse Symptoms, Findings, Diseases & Conditions > Disease Information > Major Organs-Systems > Pediatric > Disease Processes > Hereditofamilial [3]
- 383 related diseases found
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- Hereditofamilial
- Elliptocytosis, hereditary - Disease Information
- Embden-Meyerhof RBC membrane defects - Disease Information
- Encephalomyelopathy/necro/subact/Leigh - Disease Information
- Enzyme defect/deficiency disorders - Disease Information
- Epidermolysis bullosa - Disease Information
- Epidermolysis bullosa hered. letalis - Disease Information
- Epilepsy, myoclonic progressive fam'ial - Disease Information
- Erythrohepatic protoporphyria - Disease Information
- Erythropoetic protoporphyria variant - Disease Information
- Fabry disease crisis/syndrome - Disease Information
- Fabrys disease/Angiokeratatosis (trihexose ceramide) - Disease Information
- Facial ectodermal dysplasia (Setleis) - Disease Information
- Faciocardiorenal Syndrome (Eastman-Bixler) - Disease Information
- Factor IX deficiency (Christmas dis) - Disease Information
- Factor V deficiency - Disease Information
- Familial benign hypercalcemia - Disease Information
- Familial cataplexy/idiopathic - Disease Information
- Familial Cold Autoinflammatory syndrome/FCAS (1q44). - Disease Information
- Familial myeloproliferative disease - Disease Information
- Familial neutropenia - Disease Information
- Fanconi's Hereditary Renal Disease - Disease Information
- Fanconi's pancytopenia-dysmelia synd - Disease Information
- Farber disease/ceramide lipidosis - Disease Information
- Fechtner syndrome/FTNS (22q11.2) - Disease Information
- Folate malabsorption, congenital - Disease Information
- Folic acid dependency/metabolic defect - Disease Information
- Forbes disease (Cori disease, III) - Disease Information
- Formiminotransferase deficiency - Disease Information
- Fragile X syndrome/X-linked retardation - Disease Information
- Friedreich's Ataxia - Disease Information
- Fructose 1,6 diphosphatase deficiency - Disease Information
- Fructose intolerance, hereditary - Disease Information
- Fructosuria, essential - Disease Information
- Fucosidosis (Anderson-Fabry) - Disease Information
- Galactosemia - Disease Information
- Gangliosidosis, generalized (GM1) - Disease Information
- Gaucher's disease - Disease Information
- Generalized gangliosidosis/GM2 - Disease Information
- Gilles de Tourette syndrome - Disease Information
- Gittleman's syndrome - Disease Information
- Glucose 6 PD deficiency - Disease Information
- Glutamic acidemia - Disease Information
- Glutamyl-cysteine synthetase deficiency - Disease Information
- Glutaric aciduria/Acidemia - Disease Information
- Glutaric aciduria/type II - Disease Information
- Glycogen storage muscle disease/Pompe - Disease Information
- Glycogen synthetase deficiency - Disease Information
- Goldenhar syndrome - Disease Information
- Granulomatous dis/childhood, chronic - Disease Information
- Gray platelet/Hermansky-Pudlak syndrome - Disease Information
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