Individual #00001562

ID_report -
Reference -
Remarks -
Gender M
Consanguinity -
Country -
Population -
Age at death -
VIP -
Data_av -
Treatment -
Panel size 1
Diseases CSS
Owner name Gijs Santen
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-06-28 17:52:20 +02:00 (CEST)
Date last edited N/A


Phenotypes

Coffin-Siris syndrome (CSS) (CSS)   Add phenotype for this disease

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Protein     

Owner     
0000000744 - CSS generalized hypotonia; eczema (HP:0000964); no cutis marmorata (-HP:0000965); no seizures (-HP:0001250); delayed growth (HP:00001510); speech delayed (HP:0000750); cognitive impairment (HP:0100543); sparse scalp hair (HP:0002209); thick eyebrow (HP:0000574); delayed gross motor skills (HP:0002194), delayed fine motor skills (HP:0010862); no ptosis (-HP:0000520); flat (depressed/low) nasal bridge (HP:0005280), anteverted nares (HP:0000463), thick alae (HP:0009928); long philtrum (HP:0000343), wide philtrum (HP:0000289); wide mouth (HP:0000154); no cleft palate (-HP:0000175); normal ears (-HP:0000598), no ear tags (-HP:0000384); hypertrichosis (HP:0000998); wrinkling skin (HP:0007392); no scoliosis (-HP:0002650); no pectus excavatum (-HP:0000767); no dislocated elbows (-HP:0003042); no small patella (-HP:0003065); brachydactyly (HP:000156); small nails 5th only; markedly delayed bone age (HP:0003799), no prominent interphalangeal joints (-HP:0006237) , no prominent distal phalange; hypoplastic phalanges fingers/toes; joint laxity (HP:0001388); Inguinosrotal hernia; ventricular septal defect; kidney abnormality (HP:0000077); recurrent infections (HP:0002719); MRI brain normal; Isolated (sporadic) 00y11m - - - - Gijs Santen



Screenings


AscendingScreening ID     

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Owner     
0000001333 DNA SEQ - - SMARCA4 Not yet submitted Gijs Santen



Variants

Stop! No entries found!


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