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loading...| Preferred Name | Amyloidosis, Primary Cutaneous | |
| Synonyms |
Primary Localized Cutaneous Amyloidosis |
|
| ID |
http://purl.bioontology.org/ontology/MESH/C562642 |
|
| altLabel |
Primary Localized Cutaneous Amyloidosis |
|
| cui |
C0268397 |
|
| HM |
D012873 D028226 |
|
| Inverse of RB |
0 |
|
| Mapped to | ||
| MDA |
20121105 |
|
| MeSH Frequency |
169 |
|
| MMR |
20150817 |
|
| notation |
C562642 |
|
| prefLabel |
Amyloidosis, Primary Cutaneous |
|
| SC |
3 |
|
| Scope Statement |
An autosomal dominant type of familial amyloidosis that is characterized by PRURITIS and skin scratching and histologically by the finding of deposits of AMYLOID staining on keratinous debris in the papillary DERMIS. Mutations in the OSMR gene have been identified. OMIM: 105250 |
|
| TERMUI |
T801179 T801178 |
|
| TH |
OMIM (2013) |
|
| tui |
T047 |
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