Phenotypes for disease #04011 (ASNSD (asparagine synthetase deficiency (ASNSD)), OMIM:615574)

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000060436 Asparagine synthetase deficiency (OMIM:615574) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080867
0000060544 Asparagine synthetase deficiency (OMIM:615574) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080975
0000204966 Microcephaly HP:0000252 Cerebellar hypoplasia HP:0001321 - - Familial, autosomal recessive - - - - - Sandra Cooper 00267036
0000293335 Microcephaly, Apnea, Respiratory insufficiency, Seizure, Status epilepticus, Family history - - Familial, autosomal recessive 00y05m - - - - Andreas Laner 00400295
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