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congenital disorder of glycosylation Ih
Summary
- Synonym
-
- congenital disorder of glycosylation 1h
- Definition
- A congenital disorder of glycosylation I that is characterized by gastrointestinal symptoms (diarrhea, vomiting, feeding problems with failure to thrive, protein-losing enteropathy), edema and ascites (including hydrops fetalis), hepatomegaly, renal tubulopathy, coagulation anomalies due to thrombocytopenia, brain involvement (psychomotor delay, seizures, ataxia), facial dysmorphism (low-set ears and retrognathia), pes equinovarus, and muscular hypotonia and has_material_basis_in heterozygous mutation in the gene encoding dolichyl-P-glucose:Glc-1-Man-9-GlcNAc-2-PP-dolichyl-alpha-3-glucosyltransferase on chromosome 11q14.
- Super Class
- autosomal recessive disease congenital disorder of glycosylation type I
External Links
- Disease Ontology
- DOID:0080560
- Mondo Disease Ontology
- ORDO
- OMIM
- GARD
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003256 | Abnormality of the coagulation cascade |
| HP:0003642 | Type I transferrin isoform profile |
| HP:0005543 | Reduced protein C activity |
| HP:0011024 | Abnormality of the gastrointestinal tract |
| HP:0011121 | Abnormal skin morphology |
| HP:0011968 | Feeding difficulties |
| HP:0012385 | Camptodactyly |
| HP:0100678 | Premature skin wrinkling |
| HP:0003577 | Congenital onset |
| HP:0000821 | Hypothyroidism |
