Phenotypes for disease #05441 (NS1 (Noonan syndrome, type 1 (NS1)), OMIM:163950)

8 entries on 1 page. Showing entries 1 - 8.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000154292 - - 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 Familial, autosomal dominant - 9y - - - Paola Riva 00206151
0000232077 - - - Unknown - - - - - Sha Hong 00306229
0000273210 - - 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 Unknown 04y - - - - Andreas Laner 00378068
0000274662 - Noonan syndrome Short stature; heart malformation (Multiple systems) Familial - - - - - LOVD 00380809
0000302516 - - - Familial, autosomal dominant - - - - - Simin Zheng 00410414
0000302517 - - - Familial, autosomal dominant - - - - - Simin Zheng 00410415
0000321806 - - Seizure, Failure to thrive, Short stature, Neurodevelopmental delay Unknown 06y - - - - Andreas Laner 00431197
0000323703 - - Abnormality of the face, Intellectual disability, Hoarse voice, Brachydactyly, Abnormal social behavior, Slurred speech Unknown 06y - - - - Andreas Laner 00433156
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