Graham Little-Piccardi-Lassueur syndrome

General Information (adopted from Orphanet):

Synonyms, Signs: Graham Little syndrome
Piccardi-Lassueur-Little syndrome
Number of Symptoms 7
OrphanetNr: 505
OMIM Id:
ICD-10: L66.1
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset: Adult
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Alopecia
 -Rare genetic disease
 -Rare skin disease
Rare cutaneous lichen planus
 -Rare skin disease

Symptom Information: Sort by abundance 

1
 (HPO:0000989) Pruritus Frequent [Orphanet] 111 / 7739
2
 (HPO:0000962) Hyperkeratosis Very frequent [Orphanet] 216 / 7739
3
 (HPO:0002225) Sparse pubic hair Very frequent [Orphanet] 76 / 7739
4
 (HPO:0100725) Lichenification Frequent [Orphanet] 14 / 7739
5
 (HPO:0001006) Hypotrichosis Very frequent [Orphanet] 219 / 7739
6
 (HPO:0001596) Alopecia Very frequent [Orphanet] 162 / 7739
7
 (HPO:0030350) Erythematous papule Very frequent [Orphanet] 123 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: