Follicular hyperkeratosis

Symptom Information:

Symptom ID: HPO:0007502
Synonyms:
Hyperkeratosis follicularis [HPO:0007502]
Follicular hyperkeratosis [OMIM:Follicular hyperkeratosis]
Hyperkeratosis follicularis [OMIM:Hyperkeratosis follicularis]
Follicular hyperkeratosis (trunk and limbs) [OMIM:Follicular hyperkeratosis (trunk and limbs)]
Quality:
Cross references:
OMIM: "Follicular hyperkeratosis" [OMIM:Follicular hyperkeratosis]
OMIM: "Hyperkeratosis follicularis" [OMIM:Hyperkeratosis follicularis]
OMIM: "Follicular hyperkeratosis (trunk and limbs)" [OMIM:Follicular hyperkeratosis (trunk and limbs)]
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)
                            Follicular hyperkeratosis(HPO:0007502)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

BRESEK syndrome (Orphanet:85284)
Congenital muscular dystrophy, Ullrich type (Orphanet:75840)
DOWLING-DEGOS DISEASE 2 (OMIM:615327)
Ectodermal dysplasia - cutaneous syndactyly syndrome (Orphanet:247827)
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type (Orphanet:300179)
HYPERCAROTENEMIA AND VITAMIN A DEFICIENCY, AUTOSOMAL RECESSIVE (OMIM:277350)
HYPOTRICHOSIS 6 (OMIM:607903)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
PACHYONYCHIA CONGENITA 1 (OMIM:167200)
Pachyonychia congenita (Orphanet:2309)
Pilodental dysplasia - refractive errors (Orphanet:2892)