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reduced results from
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56B options
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3M
reduced results due to: symptoms, possible diagnoses, age, gender
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403200
reduced results due to: duration, diagnostic tests, modifiers
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8
options
reduced results due to: first pass, 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 - 8 of 8 diseases -
gender ?
age ?
missing left iris tissue
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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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 in skin|hearing loss|constipation|blister(s) or bump(s) on skin|stomach swelling|LIFESTYLE - Family History|delayed development|vision problems|dental problems|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, dental problems, vision problems, delayed development, life: Family History, stomach swelling
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Linear sebaceous nevus syndrome - congenital disease with distinctive birthmarks on skin
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Coloboma - congenital defect of one of the structures of the eye such as iris, retina, choroid or optic disk
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Basal-cell nevus syndrome - genetic multisystem disorder
a.k.a Multiple Basal Cell Carcinoma Syndrome, Gorlin syndrome, Gorlin-Goltz syndrome
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Coloboma of iris-anal atresia syndrome
a.k.a Cat-Eye Syndrome (CES) Schmid-Fraccaro Syndrome, Coloboma of Iris-Anal Atresia, Anal atresia
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Rieger Syndrome - rare genetic disorder affecting eyes and teeth
a.k.a Axenfeld-Rieger syndrome, Hagedoom syndrome
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Sly Syndrome - accumulation of complex carbodydrates in cells; MPS Type V11
a.k.a Mucopolysaccharidosis Type VII, MPS
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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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13q deletion syndrome - rare chromosomal disorder involving long arm of chromosome 13
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Known synonyms for your symptoms:
• defect in iris of eye -
missing iris tissue , missing right iris tissue , missing left iris tissue
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