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reduced results from
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63B options
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3M
reduced results due to: symptoms, possible diagnoses, age, gender
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446400
reduced results due to: duration, diagnostic tests, modifiers
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9
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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lifestyle modifiers
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family history of
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1 - 8 of 8 diseases -
gender ?
age ?
genu valgus
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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.
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Genu valgus - knock knees
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Pyle's disease - rare congenital disease affecting bones
a.k.a Metaphyseal dysplasia, Pyle-Cohn syndrome, Bakwin-Krida syndrome
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Aromatase deficiency - deficiency of enzyme converting male hormones to female hormones
'aromatase deficiency' is considered a medical emergency
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Camurati-Engelmann Syndrome - rare bone disorder
a.k.a diaphyseal dysplasia, Progressive Diaphyseal Dysplasia, Engelmann Syndrome
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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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Morquio Syndrome - accumulation of complex carbohydrates in cells; MPS Type 1V
a.k.a mucopolysaccharidosis IV, Morquio's
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Pierre Robin Syndrome - congenital disorder with small jaw, backward displacement of tongue and obstruction of airway
a.k.a Pierre Robin Sequence, PRS, Pierre Robin Malformation
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Ellis-van Creveld Syndrome - short limb dwarfism
a.k.a Chondroectodermal dysplasia, mesoectodermal dysplasia
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Ellis-van Creveld Syndrome
genetic or congenital
[chronic]
heart defect, heart murmur, heart murmur systolic, short stature
Ellis-van Creveld Syndrome (also called chondroectodermal dysplasia or mesoectodermal dysplasia) is a rare genetic disorder of the skeletal dysplasia type.It involves numerous anomalies including post-axial polydactyly, congenital heart defects (most commonly an atrial septal defect producing a common atrium, occurring in 60% of affected individuals), pre-natal tooth eruption, fingernail dysplasia, short-limbed dwarfism, short ribs, partial hare-lip, and malformation of the wrist bones (fusion of the hamate and capitate bones).
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For associated diagnostic procedures and therapeutic solutions, click diagnosis for details.
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Known synonyms for your symptoms:
• knock knees -
knees touch while walking , genu valgus
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