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reduced results from
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305B options
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16M
reduced results due to: symptoms, possible diagnoses, age, gender
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2M
reduced results due to: duration, diagnostic tests, modifiers
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13
reduced results due to: first pass
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8
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 - 8 of 8 diseases -
gender ?
age ?
hypopigmented patches on body
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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, washed out look, increased sweating, constipation, difficulty swallowing, urinating often
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Multiple endocrine neoplasia type 1 - disease affecting multiple endocrine glands
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Multiple endocrine neoplasia type 2b - disease affecting multiple endocrine glands
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Neurofibromatosis type 1 - inherited condition with lumps in multiple areas and dark spots on skin
a.k.a Neurofibromatosis Type I, von Recklinghausen disease, NF-1
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neurofibromatosis type 1
genetic or congenital, neurology, dermatology
[chronic with acute exacerbation]
blister(s) or bump(s) on back, lump(s) in skin, pelvic pain in females, poor coordination
Neurofibromatosis type I (NF-1), also known as von Recklinghausen syndrome, comprises, along with neurofibromatosis type II (a.k.a. MISME syndrome), tuberous sclerosis, Sturge-Weber, and Von Hippel-Lindau disease, the phakomatoses or neurocutaneous syndromes, all of which have both neurologic and dermatologic lesions.
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For associated diagnostic procedures and therapeutic solutions, click diagnosis for details.
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McCune-Albright Syndrome - genetic disease with bone, pigmentation and hormonal problems
a.k.a polyostotic fibrous dysplasia
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Turcot's Syndrome - brain tumors and colon polyps
a.k.a Turcot syndrome, Mismatch repair cancer syndrome
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Turcot's Syndrome
gastrointestinal, genetic or congenital, neurology
[chronic with acute exacerbation]
blister(s) or bump(s) on skin, blood in stool, diarrhea, painless rectal bleeding
A rare, hereditary syndrome, characterized by brain tumors (glioblastoma, astrocytoma, or spongioblastoma) associated with colonic adenomatous polyposis. The polypi vary in number from hundreds to thousands and in size; occasionally they are found in the stomach and small intestine.
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For associated diagnostic procedures and therapeutic solutions, click diagnosis for details.
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Fanconi's pancytopenia Syndrome - rare genetic disorder causing decrease in all blood forming elements
a.k.a Fanconi anemia, Fanconi pancytopenia Syndrome, Fanconi's anemia
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Ataxia-telangiectasia - progressive neurological disorder with small dilated blood vessels on skin
a.k.a AT, Boder-Sedgwick syndrome, Louis-Bar syndrome
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Pheochromocytoma - tumor of adrenal gland
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Known synonyms for your symptoms:
• cafe au lait spots -
brownish patches on body , dark patches on body , hypopigmented patches on body
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