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Phenotypes for disease #00578 (SCT (spondylocarpotarsal synostosis syndrome (SCT)), OMIM:272460)
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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Date
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Date
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Numeric
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Numeric
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22 entries on 1 page. Showing entries 1 - 22.
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Legend
How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000050411
see paper; ..., short stature; short trunk; thoracolumbar fusions; scoliosis; no cervical fusion; short neck; sacral anomaly; joint mobility limitation; clinodactyly 5th; no elbow, knee and shoulder pterygium; no single palmar crease; hearing loss; high arched/cleft palate; inguinal hernia; facial dysmorphy; no pterygium colli; no respiratory failure
spondylocarpotarsal synostosis syndrome
-
Unknown
16y
-
-
-
-
Raphael Carapito
00060275
0000050412
see paper; ..., short stature; short trunk; thoracolumbar fusions; scoliosis; cervical fusion; short neck; sacral anomaly; carpal fusion; tarsal fusion; joint mobility limitation; clinodactyly 5th; no elbow, knee and shoulder pterygium; no single palmar crease; hearing loss; high arched/cleft palate; no inguinal hernia; facial dysmorphy; no pterygium colli; no respiratory failure
spondylocarpotarsal synostosis syndrome
-
Unknown
37y
-
-
-
-
Raphael Carapito
00060260
0000050413
see paper; ..., no short stature; no short trunk; no thoracolumbar fusions; no scoliosis; cervical fusion; short neck; no sacral anomaly; carpal fusion; tarsal fusion; joint mobility limitation; clinodactyly 5th; no elbow, knee and shoulder pterygium; single palmar crease; no hearing loss; high arched/cleft palate; no inguinal hernia; facial dysmorphy; pterygium colli; no respiratory failure
multiple pterygium syndromes
-
Unknown
36y
-
-
-
-
Raphael Carapito
00060276
0000050414
see paper; ..., short stature; short trunk; thoracolumbar fusions; scoliosis; cervical fusion; short neck; sacral anomaly; carpal fusion; tarsal fusion; joint mobility limitation; no clinodactyly 5th; elbow, knee and shoulder pterygium; no single palmar crease; no hearing loss; high arched/cleft palate; inguinal hernia; facial dysmorphy; pterygium colli; respiratory failure
multiple pterygium syndromes
-
Unknown
06y
-
-
-
-
Raphael Carapito
00060277
0000186732
-
-
-
Isolated (sporadic)
-
-
-
-
-
LOVD
00247428
0000186733
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247429
0000186734
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247430
0000186735
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247431
0000186736
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247432
0000186737
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247433
0000186738
-
-
-
Isolated (sporadic)
-
-
-
-
-
LOVD
00247438
0000186739
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247440
0000186748
-
-
-
Isolated (sporadic)
-
-
-
-
-
LOVD
00247506
0000186749
-
-
-
Isolated (sporadic)
-
-
-
-
-
LOVD
00247509
0000186750
-
-
-
Isolated (sporadic)
-
-
-
-
-
LOVD
00247510
0000186751
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247512
0000186752
-
-
-
Isolated (sporadic)
-
-
-
-
-
LOVD
00247513
0000186753
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247514
0000186754
This patient shows some clinical presentation and radiological features of SCT, including multiple synostosis of cervical, thoracic, and lumbar vertebral bodies, carpal fusion, scoliosis, clinodactyly of the fifth fingers, and flat foot. Rib anomalies including rib crowding, malalignment, and uneven size and shape are rarely reported in SCT cases and are noted in this patient. Hearing loss and muscle weakness are present in this patient.
-
-
Familial
-
-
-
-
-
Chi-Fan Yang
00247516
0000204978
short stature, short neck, dysmorphic face
scoliosis, Lordosis, carpotarsal fusion
SCT
Familial, autosomal recessive
31y
31y
07y01m
07y01m
-
Samina Yasin
00267049
0000338936
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Dan Feng Fang
00449791
0000338937
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Dan Feng Fang
00449793
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