ORPHA:477759
COL4A1 or COL4A2-related cerebral small vessel disease
Synonyms: COL4A1 or COL4A2-related cerebral angiopathy
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | COL4A1 or COL4A2-related cerebral small vessel disease | COL4A1 or COL4A2-related cerebral angiopathy |
| fr | Maladie des petites artères cérébrales associée à COL4A1 ou COL4A2 | Angiopathie cérébrale associée à COL4A1 ou COL4A2 |
| de | Zerebrale Mikroangiopathie, COL4A1- oder COL4A2-abhängige | Angiopathie, zerebrale, COL4A1- oder COL4A2-abhängige |
| es | Enfermedad cerebral de pequeños vasos asociada a los genes COL4A1 o COL4A2 | Angiopatía cerebral asociada a los genes COL4A1 o COL4A2 |
| it | Angiopatia cerebrale correlata a COL4A1 o COL4A2 | |
| nl | COL4A1- of COL4A2-gerelateerde ziekte van cerebrale kleine bloedvaten | COL4A1- of COL4A2-gerelateerde cerebrale angiopathie |
| pt | Angiopatia cerebral por COL4A1 ou COL4A2 | Angiopatia cerebral por COL4A1 ou COL4A2 |
| pl | Choroba małych naczyń mózgu związana z COL4A1 lub COL4A2 | Angiopatia mózgowa związana z COL4A1 lub COL4A2 |
| cs | COL4A1 nebo COL4A2-vázaná nemoc malých cév mozku | COL4A1 or COL4A2-related cerebral angiopathy · Mozková angiopatie související s COL4A1 nebo COL4A2 |
| uk | Захворювання дрібних судин головного мозку, повязане з COL4A1 або COL4A2 | Церебральна ангіопатія, повязана з COL4A1 або COL4A2 |
| zh | COL4A1或COL4A2相关脑血管疾病 | COL4A1或COL4A2相关脑血管疾病 |
| tr | COL4A1 veya COL4A2 -ilişkili serebral küçük damar hastalığı | COL4A1 ve COL4A2-ilişkili serebral anjiyopati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18788 | E | validated | |
| UMLS | C5680103 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:477754Genetic cerebral small vessel disease
rare genetic diseases; rare neurological diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/477759
- This record as JSON: /data/d/477759.json