Disease #03906 (NS8 (Noonan syndrome, type 8 (NS-8)), OMIM:615355)

Official abbreviation NS8
Name Noonan syndrome, type 8 (NS-8)
OMIM ID 615355
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene RIT1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00043983 - PubMed: Joyce 2016 - M ? (United Kingdom (Great Britain)) - - - - - NS8 see paper; ... RIT1 RIT1 1 1 Pia Ostergaard
00043984 - PubMed: Joyce 2016 - M ? (United Kingdom (Great Britain)) - - - - - NS8 see paper; ... RIT1 RIT1 1 1 Pia Ostergaard
00080850 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - NS8 Noonan syndrome 8 (OMIM:615355) RIT1 RIT1 1 1 Daniel Trujillano
00111413 S_011 PubMed: Popp 2017, Journal: Popp 2017 - M no - - - - - - NS8 Osteogenesis imperfecta due to a de novo mutation in COL1A1, heart defect, bronchopulmonal dysplasia, tracheostoma, severe ID, short stature, facial dysmorphism RIT1 RIT1 1 1 Bernt Popp
00393308 189382 - prenatal exome analysis after ultrasound screening ? - Germany - - - - - NS8 Cystic hygroma, Fetal cystic hygroma, Edema, Hydrops fetalis, Polyhydramnios, Bilateral fetal pyelectasis, Choroid plexus cyst, Fetal choroid plexus cysts, Abnormality of ductus venosus blood flow, Abnormality of the fetal cardiovascular system RIT1 RIT1 1 1 Andreas Laner
00412206 201305 - prenatal trio-exom after ultrasound abnormalities M no Germany - - - - - NS8 Hydrops fetalis, Increased nuchal translucency, Abnormality of ductus venosus blood flow RIT1 RIT1 1 1 Andreas Laner
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