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reduced results from
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39B options
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2M
reduced results due to: symptoms, possible diagnoses, age, gender
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281600
reduced results due to: duration, diagnostic tests, modifiers
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9
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 - 9 of 9 diseases -
gender ?
age ?
preauricular skin tags
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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, hearing loss, life: Family History, overbite or underbite, delayed development, short stature
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Branchio-oto-renal syndrome - rare genetic disorder
a.k.a branciootorenal syndrome, BOR syndrome, BOR
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Schmid-Fraccaro Syndrome - cat eye syndrome: rare disorder involving chromosome 22
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Townes Syndrome - rare genetic syndrome with multiple abnormalities
a.k.a Townes–Brocks syndrome, Townes-Brocks syndrome
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11q deletion syndrome - chromosomal disorder causing delayed development and short stature
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Coffin-Siris Syndrome - rare congenital disorder with low tone and mental retardation
a.k.a Dwarfism-Onychodysplasia, Fifth Digit Syndrome, Mental Retardation with Hypoplastic 5th Fingernails and Toenails, Short Stature-Onychodysplasia.
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Goldenhar Syndrome - congenital multisystem disorder with unilateral facial anomalies
a.k.a Oculo-Auriculo-Vertebral Syndrome, OAV syndrome
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Goldenhar Syndrome
genetic or congenital
[chronic]
abnormal spine, face deformities, hearing loss
Chief markers of Goldenhar syndrome are incomplete development of the ear, nose, soft palate, lip, and mandible on usually one side of the body. Additionally, there are often issues with internal organs, especially heart, kidneys, and lungs.
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For associated diagnostic procedures and therapeutic solutions, click diagnosis for details.
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Median cleft face syndrome - rare congenital disorder
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Cri-du-chat Syndrome - syndrome that occurs from missing a piece of chromosome 5
a.k.a cri-du-chat syndrome, chromosome 5p deletion syndrome, 5p minus syndrome, Lejeune’s syndrome
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Trisomy 4p syndrome - rare chromosomal disorder
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Known synonyms for your symptoms:
• skin tags in front of ears -
preauricular skin tags , skin tags in front of right ear , skin tags in front of left ear
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