Individual #00001554

ID_report -
Reference -
Remarks -
Gender F
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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Owner     
0000000736 - CSS brith 41w, weight SD -1, OFC 32 cm; Single umbilical artery; hypotonia; no eczema (-HP:0000964); no cutis marmorata (-HP:0000965); no seizures (-HP:0001250); normal scalp hair (-HP:0100037); thick eyebrow (HP:0000574); long eyelashes (HP:0000527); normal lacrimal duct (-HP:0011481); no ptosis (-HP:0000520); no choanal stenosis (-HP:0000452); abnormality nasal bridge (HP:0000422), anteverted nares (HP:0000463), thick alae (HP:0009928); long philtrum (HP:0000343), wide philtrum (HP:0000289); wide mouth (HP:0000154); thick lower lip vermillion (HP:0000179); no cleft palate (-HP:0000175); normal ears (-HP:0000598), no ear tags (-HP:0000384); hypertrichosis (HP:0000998); no wrinkling skin (-HP:0007392); brachydactyly (HP:000156); absent 5th distal phalanx; multiple small nails (incl. 5th);; ; hypoplastic phalanges fingers/toes; aortic coarctation, PFO; MRI brain normal; Isolated (sporadic) 00y02m - - - - Gijs Santen



Screenings


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Owner     
0000001325 DNA SEQ - - ARID1B, SMARCA4, SMARCB1 Not yet submitted Gijs Santen
0000001362 DNA MLPA - - ARID1B Not yet submitted Gijs Santen



Variants

Stop! No entries found!


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