Disease #00564 (NS4 (Noonan syndrome, type 4 (NS-4)), OMIM:610733)

Official abbreviation NS4
Name Noonan syndrome, type 4 (NS-4)
OMIM ID 610733
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 SOS1
Associated tissues -
Disease features -
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Individuals

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00375527 161512 - - M - Germany - - 0 - - NS4 Cerebral hypomyelination, ptosis, normal development SOS1 - 0 1 Andreas Laner
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