Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
hypomelanosis of Ito
Summary
- Synonym
-
- Bloch-Siemans syndrome
- Incontinentia pigmenti achromians syndrome
- Ito's nevus
- incontinentia pigmenti achromians
- nevus of Ito
- Definition
- A skin disease that is characterized by distinctive skin changes, in which areas of the body lack skin color (hypopigmentation).
- Super Class
- skin disease
External Links
- Disease Ontology
- DOID:3156
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 6441 | SFTPD | surfactant protein D | |
| 10998 | SLC27A5 | solute carrier family 27 member 5 | |
| 23583 | SMUG1 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | |
| 50814 | NSDHL | NAD(P) dependent steroid dehydrogenase-like | |
| 64581 | CLEC7A | C-type lectin domain containing 7A | |
| 78989 | COLEC11 | collectin subfamily member 11 | |
| 83666 | PARP9 | poly(ADP-ribose) polymerase family member 9 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q16678 | Cytochrome P450 1B1 | |
| Q9BXN2 | C-type lectin domain family 7 member A |
