Phenotypes for disease #05102 (STROMS (Stromme syndrome (STROMS)), OMIM:243605)

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     
0000041453 Strømme syndrome - - Familial, autosomal recessive - - - - - Kaja Selmer 00054758
0000143354 Microphthalmia, Xiphoid cleft, Hydronephrosis, duodenal atresia and «apple peel» atresia - Stromme syndrome Familial, autosomal recessive - - - - - Isabel Filges 00181108
0000143370 Xiphoid cleft (HP:0100891), Renal hypoplasia (HP:0000089), duodenal atresia (HP:0002247), jejunal atresia (HP:0005235) - - Familial, autosomal recessive - - - - - Isabel Filges 00181148
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