Disease #00641 (NS7 (Noonan syndrome, type 7 (NS-7)), OMIM:613706)

Official abbreviation NS7
Name Noonan syndrome, type 7 (NS-7)
OMIM ID 613706
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene BRAF
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

3 entries on 1 page. Showing entries 1 - 3.
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00043993 - PubMed: Joyce 2016 - M - (United Kingdom (Great Britain)) - - - - - NS7 see paper; ... BRAF BRAF 1 1 Pia Ostergaard
00398754 189714 - - M no - - - - - - NS7 Failure to thrive, Abnormal hepatic echogenicity, Proptosis, Hypertonia, Low-set ears, High forehead BRAF BRAF 1 1 Andreas Laner
00410430 Patient 5 - - M no China - - - - - NS7 - BRAF BRAF 1 1 Simin Zheng
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