Disease #05440 (NS9 (Noonan syndrome, type 9 (NS-9)), OMIM:616559)

Official abbreviation NS9
Name Noonan syndrome, type 9 (NS-9)
OMIM ID 616559
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SOS2
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2018-06-20 14:52:07 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00388516 187826 - - M no Germany - - - - - NS9 Motor delay, Delayed speech and language development, Generalized amyotrophy, Scoliosis, Pectus excavatum, Flexion contracture SOS2 SOS2 1 1 Andreas Laner
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