Benign cephalic histiocytosis

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 3
OrphanetNr: 157997
OMIM Id:
ICD-10: D76.3
UMLs: C0347403
MeSH:
MedDRA:
Snomed: 255192005

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: Non-Langerhans cell histiocytosis
 -Rare skin disease

Symptom Information: Sort by abundance 

1
(HPO:0001031) Subcutaneous lipoma Very frequent [Orphanet] 112 / 7739
2
(HPO:0030350) Erythematous papule Very frequent [Orphanet] 123 / 7739
3
(OMIM) Stiff skin Very frequent [Orphanet] 31 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: