Pseudo-pelade of Brocq

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 10
OrphanetNr: 129
OMIM Id:
ICD-10: L66.0
UMLs: C0086873
MeSH: C531609
MedDRA:
Snomed: 238731001

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Not applicable
[Orphanet]
Age of onset: Adult
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Alopecia
 -Rare genetic disease
 -Rare skin disease

Symptom Information: Sort by abundance 

1
 (HPO:0100825) Cheilitis Occasional [Orphanet] 20 / 7739
2
 (HPO:0100840) Aplasia/Hypoplasia of the eyebrow Occasional [Orphanet] 117 / 7739
3
 (HPO:0001597) Abnormality of the nail Occasional [Orphanet] 115 / 7739
4
 (HPO:0001595) Abnormality of the hair Very frequent [Orphanet] 89 / 7739
5
 (HPO:0001006) Hypotrichosis Very frequent [Orphanet] 219 / 7739
6
 (HPO:0100725) Lichenification Very frequent [Orphanet] 14 / 7739
7
 (HPO:0010720) Abnormal hair pattern Very frequent [Orphanet] 14 / 7739
8
 (HPO:0200042) Skin ulcer Frequent [Orphanet] 138 / 7739
9
 (HPO:0001596) Alopecia Very frequent [Orphanet] 162 / 7739
10
 (HPO:0030350) Erythematous papule Frequent [Orphanet] 123 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: