Phenotypes for disease #01677 (MCC1D (3 methylcrotonyl-CoA carboxylase 1 deficiency (MCC1D)), OMIM:210200)

5 entries on 1 page. Showing entries 1 - 5.
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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     
0000143284 - - - Familial, autosomal recessive - - - - - Belen Perez 00181032
0000143286 - - - Familial, autosomal recessive - - - - - Belen Perez 00181034
0000143287 - - - Familial, autosomal recessive - - - - - Belen Perez 00181035
0000143324 - - - Familial, autosomal recessive - - - - - Belen Perez 00181071
0000274618 DD; ID; hypotonia; failure to thrive; acidosis (Neurological) - 3-Methylcrotonyl-CoA carboxylase 2 deficiency Familial - - - - - LOVD 00380765
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