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Differential Diagnosis For Boggy prostate, Limb ataxia/clumsiness child

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List of current finding(s):

Electromagnetic, Physics, trauma, Radiation Causes
Hypoxia
Hypoxic environment
Hypothermia, accidental/exposure
High altitude cerebral edema
Infectious Disorders (Specific Agent)
Encephalitis, Dawsons/inclusion body
Prostatoseminovesiculitis trichomonal
Infected organ, Abscesses
Seminal vesiculitis
Prostatitis, acute
Prostate abscess
Prostatitis, chronic
Granulomatous, Inflammatory Disorders
Nonbacterial prostatitis/prostatosis
Neoplastic Disorders
Cerebellar tumor
Allergic, Collagen, Auto-Immune Disorders
Acute Postinfectious Cerebellitis
Metabolic, Storage Disorders
Glucose 6 PD deficiency
Abetalipoproteinemia (Bassen Kornzweig)
Hydroxyprolinemia, congenital
Carnitine/Acylcarnitine translocase deficiency
Citrullinemia/Argininsuccinicaciduria
Combined carboxylase/Biotinidase deficiency
French-Canadian type COX mitochondrial defect
HyperArgininemia
Ketothiolase deficiency
Ketotic hyperglycinemia, idiopathic
Methylmalonic acidemia/ketotic glycine
Mitochondrial respiratory chain defects
Phenylketonuria/PKU
Propionicacidemia/ketotic glycinemia
Pyroglutamic acidemia
Pyruvate carboxylase enzyme deficiency/PCD
Infantile mitochondrial myopathy/Cox defect
Aminoacid enzyme/metabolic disorder
Beta-hydroxyisolvaleric acidemia
Glutamic acidemia
Krebs cycle/EM cycle metabolic disorder
Lysinemia
Prolinemia/type II
Proprionic acidemia/congenital
Succinic Semialdehyde dehydrogenase Deficiency
Tyrosinemia, hereditary
Valinemia/Hypervalinemia
Wilsons Disease
Carnitine palmityltranferase deficiency
Cystathioninuria
Fructose 1,6 diphosphatase deficiency
Histidinemia
Homocystinuria/homocystinemia
Hyperprolinemia
Maple syrup urine disease
Sandhoff disease
Sarcosinemia
Organic acidemias/Metabolic syndromes
Biochemical Disorders
Hypoxia, systemic, chronic
Hypoglycemia
Deficiency Disorders
Vitamin E defic. in newborns
Vitamin E deficiency
Congenital, Developmental Disorders
Asperger syndrome (mild autism)
Happy puppet syndrome/Angelman syndrome
Cerebral gigantism of childhood (Sotos)
Prader-Willi syndrome
Hereditary, Familial, Genetic Disorders
Juvenile spinal muscle atrophy (Kugelberg-Welander)
Mitochondrial myopathy/MERRF
Dominant SCA/Spinal Cerebellar ataxias
Cerebellar ataxia, congenital/hered.
Encephalomyelopathy/necro/subact/Leigh
Hereditary mitochondrial disorder
Pelizaeus-Merzbacher disease
Welander syndrome (See Kugelberg Welander)
Usage, Degenerative, Necrosis, Age Related Disorders
Primary lateral sclerosis
Relational, Mental, Psychiatric Disorders
Development impairment, childhood
Drugs
Phenothiazine dystonic/toxicity
Poisoning (Specific Agent)
Alcohol/Ethanol ingestion/intake
Lead poisoning in children
Mercury salts/bichloride acute toxicity
Mercury poisoning/infant/child
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