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Phenotypes for disease #05476 (SEMDSP (dysplasia, spondyloepimetaphyseal, SPONASTRIME type (SEMDSP)), OMIM:271510)
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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.
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
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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Date
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Numeric
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all entries containing 'South Asian', but not containing 'South East Asian'
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27 entries on 1 page. Showing entries 1 - 27.
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How to query
Phenotype ID
Diagnosis/Initial
Diagnosis/Definite
Phenotype details
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000143991
SPONASTRIME dysplasia
-
see paper; ...
Familial, autosomal recessive
07y09m
-
-
-
-
Johan den Dunnen
00183261
0000170548
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
7y9m
-
-
-
-
Johan den Dunnen
00225433
0000170549
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
7y9m
-
-
-
-
Johan den Dunnen
00225434
0000170550
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
11m
-
-
-
-
Johan den Dunnen
00225435
0000170551
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
4y9m
-
-
-
-
Johan den Dunnen
00225436
0000170552
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
9m
-
-
-
-
Johan den Dunnen
00225437
0000170553
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
22y
-
-
-
-
Johan den Dunnen
00225438
0000170558
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
5y9m
-
-
-
-
Johan den Dunnen
00225443
0000170559
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
15y7m
-
-
-
-
Johan den Dunnen
00225444
0000170560
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
14y
-
-
-
-
Johan den Dunnen
00225445
0000170561
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
15y1m
-
-
-
-
Johan den Dunnen
00225446
0000170562
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
17y10m
-
-
-
-
Johan den Dunnen
00225447
0000170563
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
4y9m
-
-
-
-
Johan den Dunnen
00225448
0000170564
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
11y
-
-
-
-
Johan den Dunnen
00225449
0000170565
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
2m
-
-
-
-
Johan den Dunnen
00225450
0000170566
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
13y
-
-
-
-
Johan den Dunnen
00225451
0000170567
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
2y2m
-
-
-
-
Johan den Dunnen
00225452
0000170568
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
2y7m
-
-
-
-
Johan den Dunnen
00225453
0000170569
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
1d
-
-
-
-
Johan den Dunnen
00225454
0000170570
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
36y
-
-
-
-
Johan den Dunnen
00225455
0000170571
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
13y
-
-
-
-
Johan den Dunnen
00225456
0000170572
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
14y
-
-
-
-
Johan den Dunnen
00225457
0000170573
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
11y
-
-
-
-
Johan den Dunnen
00225458
0000170574
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
3y5m
-
-
-
-
Johan den Dunnen
00225459
0000170575
SPONASTRIME dysplasia
-
see paper; …
Familial, autosomal recessive
1y9m
-
-
-
-
Johan den Dunnen
00225460
0000228648
Sponastrime dysplasia
Sponastrime dysplasia
Frontal bossing, saddled nasal bridge, broad nose, midface hypoplasia, low-set ears, long face, obtuse angles of the mandible, small teeth, short limbs with rhizomelia and relatively normal extremities, genua valga, flatfeet and generalized joint hypermobility.
Familial, autosomal recessive
09y
09y
-
-
-
Lucia Micale
00301520
0000333330
spondyloepimetaphyseal dysplasia,
SEMDSO
rhizomelia, disproportioned short stature, microcephaly, relative macrocephaly, increased lumbar lordosis, kyphosis, metaphyseal dysplasia
Familial, autosomal recessive
-
-
-
-
-
Murat Ozturk
00443990
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