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reduced results from
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115B options
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6M
reduced results due to: symptoms, possible diagnoses, age, gender
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816000
reduced results due to: duration, diagnostic tests, modifiers
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8
reduced results due to: first pass
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6
options
reduced results due to: final pass
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refinement options
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duration of symptoms:
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1 - 6 of 6 diseases -
gender ?
age ?
upslanting eyes
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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, heart murmur, delayed development, life: Family History, poor concentration, increased appetite
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Down's Syndrome - Trisomy 21 with delayed development and multiple defects
a.k.a Down syndrome, trisomy 21
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Noonan's Syndrome - genetic multisystem disorder with heart disease, learning problems and abnormal facial features
a.k.a Noonan Syndrome, NS
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Noonan's Syndrome
cardiac, genetic or congenital
[chronic]
face deformities, heart murmur, heart murmur systolic, limited elbow movements
Noonan Syndrome (NS) is a relatively common congenital genetic condition which affects both males and females. The principal features include congenital heart malformation, short stature, learning problems, indentation of the chest, impaired blood clotting, and a characteristic configuration of facial features.
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For associated diagnostic procedures and therapeutic solutions, click diagnosis for details.
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Prader-Willi Syndrome - type of chromosomal disorder resulting in increased appetite and learning problems
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XXXXX Syndrome - rare sex chromosome disorder with 3 extra X chromosomes
a.k.a pentasomy X, 49, XXXXX
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Femoral hypoplasia unusual facies syndrome - rare condition with absent thigh bones and abnormal facial features
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Nijmegen breakage Syndrome - rare congenital syndrome with small head and immunodeficiency
a.k.a NBS, Berlin breakage syndrome, Seemanova syndrome
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Known synonyms for your symptoms:
• upslanting eyes -
eyes upslanting
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