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

Official abbreviation CDG1Q
Name glycosylation, congenital disorder of, type Iq (CDG-1Q)
OMIM ID 612379
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene SRD5A3
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00382153 59 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - CDG1Q Oculocutaneous albinism and others; MIM, 612379 or 612713 SRD5A3 SRD5A3 1 1 LOVD
00382154 60 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - CDG1Q Oculocutaneous albinism and others; MIM, 612379 or 612713 SRD5A3 SRD5A3 1 1 LOVD
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