Phenotypes for disease #01678 (MCC2D (3-methylcrotonyl CoA carboxylase 2 deficiency (MCC2D)), OMIM:210210)

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000143288 - - - Familial, autosomal recessive - - - - - Belen Perez 00181036
0000143289 - - - Familial, autosomal recessive - - - - - Belen Perez 00181037
0000296460 see paper; ..., failure to thrive - MCC2D Familial, autosomal recessive - - 00y07m - - Johan den Dunnen 00403761
0000340278 - 3-Methylcrotonyl-CoA carboxylase 2 deficiency 3-Methylcrotonyl-CoA carboxylase 2 deficiency Familial, autosomal recessive - - - - - Miriam Erandi Reyna-Fabián 00451602
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.