Phenotypes for disease #01354 (MYHRS (Myhre syndrome (MYHRS)), OMIM:139210)

10 entries on 1 page. Showing entries 1 - 10.
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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     
0000070601 severe IDD, short stature, microcephaly, square body shape, facial dysmorphisms, cyclic vomiting, congenital kidney abnormalities, hyperammonemia, hypoglycemia, ketosis (now resolved) - - Familial, autosomal dominant - - - - - Johan den Dunnen 00092265
0000167194 MYHRS - - Unknown - - - - - Julia Lopez 00050000
0000167195 MYHRS - - Unknown - - - - - Julia Lopez 00050002
0000167244 MYHRS - - Unknown - - - - - Karl Heinimann 00218708
0000167245 MYHRS - - Unknown - - - - - Karl Heinimann 00218709
0000167246 MYHRS - - Unknown - - - - - Karl Heinimann 00218710
0000167247 MYHRS - - Unknown - - - - - Karl Heinimann 00218711
0000167248 MYHRS - - Unknown - - - - - Karl Heinimann 00218712
0000167249 MYHRS - - Unknown - - - - - Karl Heinimann 00218713
0000202115 - MYHRS - Unknown 3y - - - - Benjamin Tschupp 00264269
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