Disease #02199 (CDG2M (glycosylation, congenital disorder of, type IIm (CDG-2M)), OMIM:300896)
| Official abbreviation |
CDG2M |
| Name |
glycosylation, congenital disorder of, type IIm (CDG-2M) |
| OMIM ID |
300896 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Somatic mosaicism, X-linked dominant |
| Individuals reported having this disease |
28 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SLC35A2 |
| 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
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