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loading...| Preferred Name |
Alopecia universalis |
| Synonyms |
Atrichia, Generalized |
| ID |
http://purl.bioontology.org/ontology/MESH/C537055 |
| altLabel |
Atrichia, Generalized Generalized Atrichia Alopecia universalis congenita ALUNC Alopecia universalis congenitalis |
| cui |
C0263505 C1859877 |
| HM |
D000505 |
| Inverse of RB |
0 |
| Mapped to | |
| MDA |
20100625 |
| MeSH Frequency |
146 |
| MMR |
20190620 |
| notation |
C537055 |
| prefLabel |
Alopecia universalis |
| SC |
3 |
| Scope Statement |
A genetically determined, immune-mediated disorder of the HAIR FOLLICLE and one of the most common human AUTOIMMUNE DISEASES. Severity ranges from patchy localized hair loss on the SCALP to the complete absence of hair everywhere on the body. This phenotype has been mapped to chromosome 18 (OMIM: 104000) and a mutation in the HR gene has also been identified (OMIM: 203655). |
| TERMUI |
T741313 T741318 T807695 T741315 T000961642 |
| TH |
ORD (2010) OMIM (2013) NLM (2019) |
| tui |
T019 T047 |
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