Phenotypes for disease #02654 (LIS1 (lissencephaly, type 1 (LIS-1)), OMIM:607432)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000340197 - HMG-CoA lyase deficiency HMG-CoA lyase deficiency Familial, autosomal recessive - 00y05m09d - - - Miriam Erandi Reyna-Fabián 00451460
0000340199 Cerebral cortical atrophy, hypsarrhythmia, moderate intellectual disability Hyperbeta-alaninemia Lissencephaly 1 Familial, autosomal dominant - - - - - Miriam Erandi Reyna-Fabián 00451462
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