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Phenotypes for disease #02878 (SCDO3 (dysostosis, spondylocostal, autosomal recessive, type 3 (SCDO-3)), OMIM:609813)
Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Inheritance
: Indicates the inheritance of the phenotype in the family; unknown, familial (autosomal/X-linked, dominant/ recessive), paternal (Y-linked), maternal (mitochondrial), isolated (sporadic) or complex
All options:
Unknown
Familial
Familial, autosomal dominant
Familial, autosomal recessive
Familial, X-linked
Familial, X-linked dominant
Familial, X-linked dominant, male sparing
Familial, X-linked recessive
Paternal, Y-linked
Maternal, mitochondrial
Isolated (sporadic)
Di-genic
Complex
- = Not applicable
Age/Examination
: age at which the individual was examined.
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Diagnosis
: age diagnosis was confirmed
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Onset
: Age first symptoms disease appeared in individual:
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Phenotype/Onset
: individual's phenotype at Age/Onset described using HPO
Protein
: result from protein staining
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space
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=""
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combination
Text
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Date
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Date
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Date
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Date
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Date
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Date
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Date
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Date
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Numeric
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Numeric
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Numeric
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Numeric
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>
Numeric
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Numeric
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combination
Numeric
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all entries with values from 20 to 29, but not equal to 23
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Example
Matches
Asian
all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
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all entries containing 'Asian' but not containing 'Caucasian'
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all entries containing 'Asian' or 'African', but not containing 'Caucasian'
"South Asian"
all entries containing 'South Asian', but not containing 'South East Asian'
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4 entries on 1 page. Showing entries 1 - 4.
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How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000318904
Polyhydramnios HP:0001561 Respiratory distress HP:0002098 Kyphoscoliosis HP:0002751 Rib fusion HP:0000902 Hemivertebrae HP:0002937 Thoracic dysplasia HP:0006644 Pulmonary hypoplasia HP:0002089 Absent/hypoplastic coccyx HP:0008436
skeletal dysplasia
Spondylocostal dysostosis 3
Familial, autosomal recessive
00y01m
-
-
prenatal
Beta-1,3-N-acetylglucosaminyltransferase lunatic fringe
Edoardo Errichiello
00427959
0000318905
Respiratory distress HP:0002098 Hemivertebrae HP:0002937 Vertebral fusion HP:0002948
skeletal dysplasia
Spondylocostal dysostosis 3
Familial, autosomal recessive
-
-
-
-
Beta-1,3-N-acetylglucosaminyltransferase lunatic fringe
Edoardo Errichiello
00427960
0000318906
Spinal dysraphism HP:0010301 Hemivertebrae HP:0002937 Rib fusion HP:0000902 Short stature HP:0004322 Pectus carinatum HP:0000768 Butterfly vertebrae HP:0003316 Pulmonary hypoplasia HP:0002089
skeletal dysplasia
Spondylocostal dysostosis 3
Familial, autosomal recessive
-
-
-
-
Beta-1,3-N-acetylglucosaminyltransferase lunatic fringe
Edoardo Errichiello
00427961
0000321934
Short stature (10th to 25th %), vertebral segmental defects and rib fusions (9 right ribs and 10 left), left 38-degree scoliosis at L1/S1, 44-degree lordosis at L1/S1, and 32-degree kyphosis at T2/T12.
-
-
Familial, autosomal recessive
-
-
-
-
-
Parker Cole Wengryn
00431334
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