Phenotypes for disease #01663 (ASAD (argininosuccinic aciduria deficiency), OMIM:207900)

7 entries on 1 page. Showing entries 1 - 7.
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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     
0000060505 Argininosuccinic aciduria (OMIM:207900) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080936
0000086073 late-onset - - Isolated (sporadic) - - - - - Johan den Dunnen 00108494
0000086074 neonatal-onset - - Isolated (sporadic) - - - - - Johan den Dunnen 00108524
0000086075 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00108525
0000187302 see paper; … ASL deficiency - Familial, autosomal recessive - - - - - Johan den Dunnen 00248293
0000187303 see paper; … ASL deficiency - Familial, autosomal recessive - - - - - Johan den Dunnen 00248294
0000339532 Moderate intellectual disability Argininosuccinic aciduria argininosuccinic aciduria deficiency Familial, autosomal recessive - <00y00m02d - - - Miriam Erandi Reyna-Fabián 00450472
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