Phenotypes for disease #00902 (CDG1Q (glycosylation, congenital disorder of, type Iq (CDG-1Q)), OMIM:612379)

2 entries on 1 page. Showing entries 1 - 2.
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     
0000275995 Oculocutaneous albinism and others; MIM, 612379 or 612713 MIM, 612379 or 612713 - Familial, autosomal recessive - - - - - LOVD 00382153
0000275996 Oculocutaneous albinism and others; MIM, 612379 or 612713 MIM, 612379 or 612713 - Familial, autosomal recessive - - - - - LOVD 00382154
Legend   How to query  


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