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reduced results from
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302B options
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16M
reduced results due to: symptoms, possible diagnoses, age, gender
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2M
reduced results due to: duration, diagnostic tests, modifiers
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23
reduced results due to: first pass
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7
options
reduced results due to: final pass
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refinement options
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duration of symptoms:
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lifestyle modifiers
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family history of
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1 - 7 of 7 diseases -
gender ?
age ?
concavity in breastbone
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score graph
The score graph represents the results on the x axis and the "score" on the y axis. The purpose of this graph is to visually display the relative scores and how dramatically or not the likelihood of the diseases compare.
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Show only results from category
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weighted category breakdown
This pie chart represents the results broken down categorically. The size of the pie, or "score" of the category, is the sum of the scores of the diseases in the category. Please note a disease may fall into multiple category.
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variable sensitivity
This bar chart represents the variables that the results and their ordering are most sensitive too.
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The results should NOT be considered a diagnosis.
Please consult your health care provider.
edit important variables such as:
demo: duration, demo: age, difficulty breathing, palpitations, palpitations without fever, heart rate irregular, cataract
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Idiopathic scoliosis - lateral curvature of spine
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Mitral valve prolapse - displacement of part of valve that separates the left upper and lower chambers of the heart
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Turner's Syndrome - chromosomal condition causing underdevelopment of female sex characteristics
a.k.a Turner syndrome, Ullrich-Turner syndrome
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Holt-Oram Syndrome - inherited disorder with abnormal bones and heart disease
a.k.a Chudley-Mccullough Syndrome, Atriodigital dysplasia, Cardiac Limb Syndrome, Heat hand Syndrome, Ventriculo-Radial syndrome
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Homocystinuria - multisystem metabolic disease due to abnormal methionine metabolism
a.k.a Cystathionine beta synthase deficiency
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homocystinuria
cardiovascular, genetic or congenital, hematological, metabolic, muscles, musculoskeletal and connective tissue disorders, neurological
[chronic]
anemia, curvature of spine, delayed development, pain in leg(s)
Homocystinuria, also known as Cystathionine beta synthase deficiency, is an inherited disorder of the metabolism of the amino acid methionine. It is an inherited autosomal recessive trait, which means a child needs to inherit the defective gene from both parents to be affected.
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For associated diagnostic procedures and therapeutic solutions, click diagnosis for details.
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Congenital myopathies - inherited muscle diseases
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Osteogenesis imperfecta type I - genetic bone disease causing frequent fractures
a.k.a Brittle Bone Disease, Lobstein syndrome
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Known synonyms for your symptoms:
• depression in breast bone -
sunken breast bone , breast bone depressed , concavity in breastbone , sternum depressed , sternum sunken , sternum concavity , funnel chest , pectus excavatum
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