Disease #00682 (NS3 (Noonan syndrome, type 3 (NS-3)), OMIM:609942)

Official abbreviation NS3
Name Noonan syndrome, type 3 (NS-3)
OMIM ID 609942
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene KRAS
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

4 entries on 1 page. Showing entries 1 - 4.
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00043991 - PubMed: Joyce 2016 - M - (United Kingdom (Great Britain)) - - - - - NS3 see paper; ... KRAS KRAS 1 1 Pia Ostergaard
00043992 - PubMed: Joyce 2016 - M - (United Kingdom (Great Britain)) - - - - - NS3 see paper; ... KRAS KRAS 1 1 Pia Ostergaard
00111412 S_009 PubMed: Popp 2017, Journal: Popp 2017 - F no - - - - - - NS3 Severe speech delay, moderate ID, behavioral anomalies, normal growth, facial dsymorphism, low set ears KRAS KRAS 1 1 Bernt Popp
00416979 205573 - prenatal trio-exom after ultrasound abnormalities M no Germany - - - - - NS3 Hydronephrosis, Single umbilical artery, Abnormality of prenatal development or birth, Intrauterine growth retardation, Hydrops fetalis, Fetal ascites, Atrioventricular canal defect, Fetal cystic hygroma, Fetal pyelectasis, Fetal hydrothorax KRAS KRAS 1 1 Andreas Laner
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