Disease #00575 (NS5 (Noonan syndrome, type 5 (NS-5)), OMIM:611553)

Official abbreviation NS5
Name Noonan syndrome, type 5 (NS-5)
OMIM ID 611553
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 3
Associated with 1 gene RAF1
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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00081007 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - NS5 Noonan syndrome 5 (OMIM:611553) RAF1 RAF1 1 1 Daniel Trujillano
00306221 125 - - M - China - - - - - NS5 - RAF1 RAF1 1 1 Sha Hong
00410416 Patient 3 - - M no China - - - - - NS5 - RAF1 RAF1 1 1 Simin Zheng
00410417 Patient 4 - - M no China - - - - - NS5 - RAF1 RAF1 1 1 Simin Zheng
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