Perifollicular hyperkeratosis

Symptom Information:

Symptom ID: HPO:0007468
Synonyms:
Hyperkeratosis [HPO:0007468]
Hyperkeratosis (especially extensor surfaces) [OMIM:Hyperkeratosis (especially extensor surfaces)]
Hyperkeratosis (in some patients) [OMIM:Hyperkeratosis (in some patients)]
Hyperkeratosis (palms, soles, elbows, knees) [OMIM:Hyperkeratosis (palms, soles, elbows, knees)]
Quality:
Cross references:
OMIM: "Hyperkeratosis (especially extensor surfaces)" [OMIM:Hyperkeratosis (especially extensor surfaces)]
OMIM: "Hyperkeratosis (in some patients)" [OMIM:Hyperkeratosis (in some patients)]
OMIM: "Hyperkeratosis (palms, soles, elbows, knees)" [OMIM:Hyperkeratosis (palms, soles, elbows, knees)]
UMLS:C0870082 "Hyperkeratosis" [HPO:0007468]
Is a (Direct Parents):
HPO         Hyperkeratosis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of skin morphology(HPO:0011121)
                   Thickened skin(HPO:0001072)
                      Epidermal thickening(HPO:0011368)
                         Hyperkeratosis(HPO:0000962)
                            Perifollicular hyperkeratosis(HPO:0007468)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME (OMIM:615510)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT (OMIM:148210)
Monilethrix (Orphanet:573)