Phenotypes for disease #00229 (PWS (Prader-Willi syndrome (PWS)), OMIM:176270)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000030653 Not Rett synd. - Prader-Willi syndrome - - Unknown - - - - - RettBASE 00040370
0000231248 Makrosomie, Adipositas - - Unknown - - - - - Andreas Laner 00305399
0000357047 0001511: Intrauterine growth retardation, 001531: Growth retardation in infants, 0001319: Neonatal hypotonia, 0001290: Generalised hypotonia, 0008872: Eating disorders in children Congenital myopathy PWS Isolated (sporadic) - - - - - Camille Verebi 00472238
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