Cutaneous lupus erythematosus
General Information (adopted from Orphanet):
Synonyms, Signs:
|
|
Number of Symptoms
|
20
|
OrphanetNr:
|
535
|
OMIM Id:
|
|
ICD-10:
|
L93
|
UMLs:
|
C0024137
|
MeSH:
|
D008178
|
MedDRA:
|
10056509
|
Snomed:
|
7119001
|
Prevalence, inheritance and age of onset:
Prevalence:
|
50
of 100 000
[Orphanet]
|
Inheritance:
|
Multifactorial
[Orphanet]
|
Age of onset:
|
All ages
[Orphanet]
|
Disease classification (adopted from Orphanet):
Parent Diseases:
|
Autoimmune disease with skin involvement
-Rare skin disease
|
|
|
|
|
|
|
|
|
1
|
(HPO:0005059)
|
Arthralgia/arthritis |
Very frequent [Orphanet]
|
|
|
|
141 / 7739
|
2
|
(HPO:0100585)
|
Telangiectasia of the skin |
Very frequent [Orphanet]
|
|
|
|
66 / 7739
|
3
|
(HPO:0200042)
|
Skin ulcer |
Very frequent [Orphanet]
|
|
|
|
138 / 7739
|
4
|
(HPO:0000992)
|
Cutaneous photosensitivity |
Occasional [Orphanet]
|
|
|
|
75 / 7739
|
5
|
(HPO:0003765)
|
Psoriasis |
Very frequent [Orphanet]
|
|
|
|
17 / 7739
|
6
|
(HPO:0010783)
|
Erythema |
Very frequent [Orphanet]
|
|
|
|
138 / 7739
|
7
|
(HPO:0000988)
|
Skin rash |
Very frequent [Orphanet]
|
|
|
|
98 / 7739
|
8
|
(HPO:0000962)
|
Hyperkeratosis |
Very frequent [Orphanet]
|
|
|
|
216 / 7739
|
9
|
(HPO:0000989)
|
Pruritus |
Very frequent [Orphanet]
|
|
|
|
111 / 7739
|
10
|
(HPO:0011123)
|
Inflammatory abnormality of the skin |
Very frequent [Orphanet]
|
|
|
|
10 / 7739
|
11
|
(HPO:0007400)
|
Irregular hyperpigmentation |
Very frequent [Orphanet]
|
|
|
|
72 / 7739
|
12
|
(HPO:0200037)
|
Skin vesicle |
Very frequent [Orphanet]
|
|
|
|
102 / 7739
|
13
|
(HPO:0001063)
|
Acrocyanosis |
Very frequent [Orphanet]
|
|
|
|
56 / 7739
|
14
|
(HPO:0001031)
|
Subcutaneous lipoma |
Very frequent [Orphanet]
|
|
|
|
112 / 7739
|
15
|
(HPO:0000958)
|
Dry skin |
Very frequent [Orphanet]
|
|
|
|
152 / 7739
|
16
|
(HPO:0000969)
|
Edema |
Very frequent [Orphanet]
|
|
|
|
117 / 7739
|
17
|
(HPO:0012740)
|
Papilloma |
Occasional [Orphanet]
|
|
|
|
17 / 7739
|
18
|
(OMIM)
|
Stiff skin |
Very frequent [Orphanet]
|
|
|
|
31 / 7739
|
19
|
(MedDRA:10025421)
|
Macule |
Very frequent [Orphanet]
|
|
|
|
55 / 7739
|
20
|
(HPO:0030350)
|
Erythematous papule |
Very frequent [Orphanet]
|
|
|
|
123 / 7739
|
ClinVar (via SNiPA)
Gene symbol |
Variation |
Clinical significance |
Reference |