Disease #05854 (NS2 (Noonan syndrome, type 2 (NS2)), OMIM:605275)

Official abbreviation NS2
Name Noonan syndrome, type 2 (NS2)
OMIM ID 605275
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene LZTR1
Associated tissues -
Disease features -
Remarks -
Date created 2020-10-16 09:46:56 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00428256 211995 - - F yes - - - - - - NS2 Hypertrophic cardiomyopathy, Feeding difficulties in infancy, Cardiomyopathy, sister died at 10 month of cardiomyopathy LZTR1 LZTR1 1 1 Andreas Laner
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