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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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MIRAGE
Wolf-Hirschhorn syndrome
Summary
- Synonym
-
- 4p deletion syndrome
- PITT SYNDROME
- Pitt-Rogers-Danks Syndrome
- chromosome 4p16.3 deletion syndrome
- Definition
- A chromosomal deletion syndrome that is characterized by distinct craniofacial features, hypotonia and intellectual disability and has_material_basis_in a hemizygous deletion of chromosome 4p16.3.
- Super Class
- chromosomal deletion syndrome
External Links
- Disease Ontology
- DOID:0050460
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- GARD
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q91V87 | Fibroblast growth factor receptor-like 1 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000028 | Cryptorchidism |
| HP:0000047 | Hypospadias |
| HP:0000077 | Abnormality of the kidney |
| HP:0000078 | Abnormality of the genital system |
| HP:0000079 | Abnormality of the urinary system |
| HP:0000153 | Abnormality of the mouth |
| HP:0000159 | Abnormal lip morphology |
| HP:0000175 | Cleft palate |
| HP:0000204 | Cleft upper lip |
| HP:0000252 | Microcephaly |
