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Woolly hair

Disease Export to PDF
Name:
Woolly hair
Description:
A rare congenital skin disease defined as an abnormality of the structure of the scalp hair and characterized by extreme kinkiness of the hair.
ORPHAcode:
170
Synonyms:
Familial woolly hair syndrome
Familial wooly hair syndrome
Hereditary woolly hair syndrome
Hereditary wooly hair syndrome
Wooly hair
XREF(s):
Orphanet
MeSH
ICD-10
OMIM
OMIM
OMIM
OMIM
OMIM
MedDRA
Analyte(s):
LPAR6
LIPH
KRT74
KRT71
KRT25
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14