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reduced results from
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42B options
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2M
reduced results due to: symptoms, possible diagnoses, age, gender
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300000
reduced results due to: duration, diagnostic tests, modifiers
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5
reduced results due to: first pass
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3
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 - 3 of 3 diseases -
gender ?
age ?
skin light or fair
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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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|bruises on foot (feet)|bruises on face|anemia|swollen leg|pain in leg(s)|delayed development|curvature of spine|cataract|urinating less than normal|urinating large amounts|not gaining weight|increased thirst|LIFESTYLE - Family History|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, life: Family History, increased thirst, not gaining weight, urinating large amounts, urinating less than normal
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Cystinosis - accumulation of type of aminoacid in body tissues
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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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Hermansky Pudlak Syndrome - inherited multisystem disease causing decreased pigmentation and bleeding
a.k.a Hermansky-Pudlak Syndrome, HPS, Albinism occulocutaneous, Platelet defects
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for more please login, login is free (click to login)
Known synonyms for your symptoms:
• fair or light skin -
skin light or fair
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