Individual #00001565

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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Protein     

Owner     
0000000747 - CSS brith 39w, weight SD 0.2; Colpocephaly, strabismus, fetal pads; eczema (HP:0000964); no cutis marmorata (-HP:0000965); no seizures (-HP:0001250); no growth abnormality (-HP:0001507); abnormal vision (HP:0000504); no hearing loss (-HP:0000365); severe speech delay (HP:0000750); moderate intellectual disability; normal scalp hair (-HP:0100037); thick eyebrow (HP:0000574); delayed gross motor skills (HP:0002194), delayed fine motor skills (HP:0010862); normal lacrimal duct (-HP:0011481); no ptosis (-HP:0000520); no choanal stenosis (-HP:0000452); normal nasal bridge (-HP:0000422), no anteverted nares (-HP:0000463); normal philtrum (-HP:0000288); wide mouth (HP:0000154); no cleft palate (-HP:0000175); normal ears (-HP:0000598), no ear tags (-HP:0000384); hypertrichosis (HP:0000998); no scoliosis (-HP:0002650); pectus excavatum (HP:0000767); no dislocated elbows (-HP:0003042); no brachydactyly (-HP:000156); absent 5th distal phalanx; small nails 5th only;; ; hypoplastic phalanges fingers/toes; no joint laxity (-HP:0001388); constipation; no cardiac abnormality (-HP:0001627); no kidney abnormality (-HP:0000077); agenesis corpus callosum (HP:0001274); strabismus (HP:0000486) Isolated (sporadic) ? - - - - Gijs Santen



Screenings


AscendingScreening ID     

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Owner     
0000001336 DNA SEQ - - - Not yet submitted Gijs Santen



Variants

Stop! No entries found!


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