Disease #05441 (NS1 (Noonan syndrome, type 1 (NS1)), OMIM:163950)

Official abbreviation NS1
Name Noonan syndrome, type 1 (NS1)
OMIM ID 163950
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 8
Phenotype entries for this disease 8
Associated with 1 gene PTPN11
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2018-06-20 14:58:17 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00206151 - - - F no Italy - - - - - NS1 a myopathic appearance of the face with bilateral ptosis was evident, a high forehead, micrognatia, and slight webbing, Abnormalities of skin pigmentation included cafe-au-lait spots, lentigines and vitiligo areas SOS1 SOS1 1 1 Paola Riva
00306229 136 - - M - China - - - - - NS1 - PTPN11 PTPN11 1 1 Sha Hong
00378068 181296 - - F no Germany - - - - - NS1 Abnormal palate morphology, High palate, Microcephaly, Deeply set eye, Aplasia/Hypoplasia of the cerebrum, Abnormality of higher mental function, Decreased head circumference, Cognitive impairment, Abnormality of globe location PTPN11 PTPN11 1 1 Andreas Laner
00380809 ? PubMed: Nair 2018 - ? - Lebanon - - - - - NS1 Short stature; heart malformation (Multiple systems) - PTPN11 1 1 LOVD
00410414 Patient 1 - - M no China - - - - - NS1 - PTPN11 PTPN11 1 1 Simin Zheng
00410415 Patient 2 - - M no China - - - - - NS1 - PTPN11 PTPN11 1 1 Simin Zheng
00431197 212980 - - F no Germany - - - - - FFEVF3, NS1 Seizure, Failure to thrive, Short stature, Neurodevelopmental delay NPRL3, PTPN11 NPRL3, PTPN11 2 1 Andreas Laner
00433156 250856 - - M no Germany - - - - - NS1 Abnormality of the face, Intellectual disability, Hoarse voice, Brachydactyly, Abnormal social behavior, Slurred speech PTPN11 PTPN11 1 1 Andreas Laner
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