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Medical Subject Headings
Last uploaded:
August 28, 2024
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| Preferred Name | Dyschromatosis universalis hereditaria | |
| Synonyms |
|
|
| ID |
http://purl.bioontology.org/ontology/MESH/C535730 |
|
| cui |
C2930995
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|
| Has mapping qualifier | ||
| HM |
D012873 D010859/Q000151
|
|
| Inverse of RB |
0
|
|
| Mapped to | ||
| MDA |
20100825
|
|
| MeSH Frequency |
29
|
|
| MMR |
20160929
|
|
| notation |
C535730
|
|
| prefLabel |
Dyschromatosis universalis hereditaria
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|
| SC |
3
|
|
| Scope Statement |
A rare herditary skin condition characterized by hyper- and hypopigmented macules of variable size and shape that appear in infancy or early childhood on the trunk, limbs, and sometimes the face. There may also be abnormalities affecting the hair, nails, and dermal connective tissue as well as nerves. OMIM: 127500
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|
| TERMUI |
T737014
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|
| TH |
ORD (2010)
|
|
| tui |
T047
|
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