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Differential Diagnosis For Swimming infant reflex/Abnormal, Virilism


List of current finding(s):

Trauma Causes
Birth canal injury, newborn
Spinal cord injury
Infectious Disorders (Specific Agent)
Newborn TORCH syndrome
Poliomyelitis, paralytic, spinal
Infected organ, Abscesses
Acute infection
Newborn Sepsis Syndrome
Sepsis, overwhelming
Neoplastic Disorders
Ovarian neoplasm
Adrenal neoplasm
Carcinoma, adrenal cortex
Lutein cell tumor ovary
Ovarian Dysgerminoma
Ovarian/masculinizing tumor
Ovary hilar cell tumor
Ovary, arrhenoblastoma
Pituitary adenoma, ACTH secreting
Allergic, Collagen, Auto-Immune Disorders
Guillain-Barre syndrome
Isaacs potassium channel myopathy syndrome
Metabolic, Storage Disorders
Tay-Sachs disease
Combined carboxylase/Biotinidase deficiency
Cytochrome C Oxidase Deficiency/COX Complex Defect
French-Canadian type COX mitochondrial defect
Infantile mitochondrial myopathy/Cox defect
Cerebral Gaucher's of infants (acute)
Cerebral lipidosis disorder
LCHAD/Long chain OH-CoA dehydrogenase def
MCAD/Medium chain OH-CoA Dehydrogenase def
VLCHAD/Very Long chain OH-CoA dehydrogenase def
Achard-Thiers syndrome
Carnitine deficiency syndrome
Glutaric aciduria/type II
Glycogen storage diseases
Glycogen storage muscle disease/Pompe
Mucolipidosis IV (Bermans Syndrome)
Tetrahydrobiopterin deficiency/Atypical PKU
Von Gierke's disease/glycogenosis I
Aromatase Deficiency Syndrome
Lysosome Storage Disease
Biochemical Disorders
Congenital, Developmental Disorders
Down's Syndrome
Adrenogenital syndrome
Allan-Herndon Mental Retardation/X-linked
Shprintzen-Goldberg craniosynostosis syndrome (15q21.1)
Amyotonia, congenita
Hypotonia of Werdnig-Hoffman
Prader-Willi syndrome
Birth asphyxia Syndrome/Hypoxic event
Central Hypotonia Infants
Coffin-Lowry Syndrome
Hereditary, Familial, Genetic Disorders
Hereditary neuropathy
Muscular dystrophy
Spinal muscle atrophy
Spinal muscle atrophy, infantile
Chromosome 22q13.3 deletion syndrome (22q13.3)
Juvenile spinal muscle atrophy (Kugelberg-Welander)
Mitochondrial myopathy/MERRF
Beckwith-Wiedemann Syndrome
Zellweger Cerebrhepatorenal syndrome
Dominant SCA/Spinal Cerebellar ataxias
Borjeson-Forssman-Lehmann Syn/BFLS (xq26.3)
Central core disease
Cerebellar ataxia, congenital/hered.
Dysautonomia, familial
Leukodystrophy, Krabbe
Lipodystrophy, generalized
Muscular atrophy, infantile, spinal
Myotonia congenita (Thomsens d.)
Nemaline myopathy
Oculocerebrorenal dystrophy/Lowe syndrome
Progressive spinal muscular atrophy
Abducted thumbs syndrome
Hereditary dysmyelinating neuropathy
Hereditary sensory neuropathy (type II)
Myopathy, Desmin Storage type/Sarcoplasmin bodies
Myopathy, Myotubular/Centronuclear
Say Syndrome 1
Welander syndrome (See Kugelberg Welander)
Vegetative, Autonomic, Endocrine Disorders
Acromegaly (Gigantism)
Adrenogenital syndrome, acquired
Myasthenia gravis
Polycystic ovaries/Stein-Leventhal
Virilism syndrome
Neonatal myasthenia
Benzodiazepines Administration/Toxicity
Progestins Administration/Toxicity
Benzodiazepine toxicity/overdose
Ciclosporine (Sandimmune) Administration/Toxicity
Minoxidil (Loniten) Administration/Toxicity
Anabolic steroid hormone Administration/Toxicity
Danazol (Danocrine) Administration/Toxicity
Drospirenone (Progestin) Administration/Toxicity
Poisoning (Specific Agent)
Botulism, infant