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Repository for lectin-assisted multimodality data
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MIRAGE
congenital disorder of glycosylation Ik
Summary
- Synonym
-
- congenital disorder of glycosylation 1k
- Definition
- A congenital disorder of glycosylation I that is characterized by severe developmental and psychomotor delay, muscular hypotonia, intractable early-onset seizures, and microcephaly and has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding beta-1,4-mannosyltransferase on chromosome 16p13.
- Super Class
- autosomal recessive disease congenital disorder of glycosylation type I
External Links
- Disease Ontology
- DOID:0080563
- Mondo Disease Ontology
- ORDO
- GARD
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002808 | Kyphosis |
| HP:0001252 | Hypotonia |
| HP:0001560 | Abnormality of the amniotic fluid |
| HP:0000239 | Large fontanelles |
| HP:0001290 | Generalized hypotonia |
| HP:0000135 | Hypogonadism |
| HP:0001744 | Splenomegaly |
| HP:0003642 | Type I transferrin isoform profile |
| HP:0000316 | Hypertelorism |
| HP:0001511 | Intrauterine growth retardation |
