Phenotypes for disease #00578 (SCT (spondylocarpotarsal synostosis syndrome (SCT)), OMIM:272460)

22 entries on 1 page. Showing entries 1 - 22.
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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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