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reduced results from
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131B options
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4M
reduced results due to: symptoms, possible diagnoses, age, gender
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608000
reduced results due to: duration, diagnostic tests, modifiers
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10
reduced results due to: first pass
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2
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 - 2 of 2 diseases -
gender ?
age ?
arms or legs long and thin
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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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 or bump(s) on face|blister(s) or bump(s) on eyelid(s)|blister(s) or bump(s) in mouth|passed out but now well|palpitations without fever|palpitations|curvature of spine|cataract|DEMOGRAPHIC - age|DEMOGRAPHIC - duration|)
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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, cataract, curvature of spine, palpitations, palpitations without fever, passed out but now well
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Multiple endocrine neoplasia type 2b - disease affecting multiple endocrine glands
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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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Known synonyms for your symptoms:
• long thin extremities -
long thin arms or legs , extremities long and thin , limbs long and thin , arms or legs long and thin
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