Phenotypes for disease #05161

9 entries on 1 page. Showing entries 1 - 9.
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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     
0000050839 Fryns syndrome diagnosed prenatally - - Familial, autosomal recessive - - - - - Aideen McInerney-Leo 00063836
0000050840 - - - Familial, autosomal recessive - - - - - Aideen McInerney-Leo 00063837
0000128893 - - - Familial, autosomal recessive - - - - - Philippe Campeau 00163766
0000128894 - - - Familial, autosomal recessive - - - - - Philippe Campeau 00163767
0000128895 - - - Familial, autosomal recessive - - - - - Philippe Campeau 00163768
0000128896 - - - Familial, autosomal recessive - - - - - Philippe Campeau 00163769
0000128897 - - - Familial, autosomal recessive - - - - - Philippe Campeau 00163771
0000128898 - - - Familial, autosomal recessive - - - - - Philippe Campeau 00163773
0000143367 Dandy Walker malformation (HP:0001305), Renal dysplasia (HP:0000110), Hydronephrosis (HP:0000126), Diaphragmatic hernia (HP:0000776) - - Familial, autosomal recessive - - - - - Isabel Filges 00181145
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