Erythroderma

Symptom Information:

Symptom ID: HPO:0001019
Synonyms:
Generalized erythroderma [HPO:0001019]
Generalized erythrodermia [HPO:0001019]
Erythema [Orphanet:23260]
Erythematous condition (disorder) [Orphanet:23260]
Erythema (morphologic abnormality) [Orphanet:23260]
Erythema of skin (finding) [Orphanet:23260]
Erythema (finding) [Orphanet:23260]
Generalized erythroderma (disorder) [Orphanet:23260]
Erythrodermic eczema (disorder) [Orphanet:23260]
Erythroderma (disorder) [Orphanet:23260]
Exfoliative dermatitis [Orphanet:23260]
Erythroderma [OMIM:Erythroderma]
Generalized erythroderma [OMIM:Generalized erythroderma]
Generalized erythrodermia [OMIM:Generalized erythrodermia]
Erythema/erythematous lesions/erythroderma/polymorphous erythema [Orphanet:23260]
Erythema [MedDRA:10015150]
Erythema auricular [MedDRA:10015150]
Erythema circumocular-blepharal [MedDRA:10015150]
Erythema diffuse [MedDRA:10015150]
Erythema facial [MedDRA:10015150]
Erythema NOS [MedDRA:10015150]
Erythema oedematous [MedDRA:10015150]
Erythematous conditions [MedDRA:10015150]
Face red [MedDRA:10015150]
Localized erythema [MedDRA:10015150]
Lower legs erythematous [MedDRA:10015150]
Other specified erythematous condition [MedDRA:10015150]
Other specified erythematous conditions [MedDRA:10015150]
Red face [MedDRA:10015150]
Red neck [MedDRA:10015150]
Redness [MedDRA:10015150]
Redness facial [MedDRA:10015150]
Redness of external ear [MedDRA:10015150]
Redness of face [MedDRA:10015150]
Redness of legs [MedDRA:10015150]
Skin erythema [MedDRA:10015150]
Skin hyperaemia [MedDRA:10015150]
Skin hyperemia [MedDRA:10015150]
Skin red [MedDRA:10015150]
Unspecified erythematous condition [MedDRA:10015150]
Erythema periorbital [MedDRA:10015150]
Redness in breast [MedDRA:10015150]
Erythema ear [MedDRA:10015150]
Erythema edematous [MedDRA:10015150]
Infiltrative erythema [MedDRA:10015150]
Localised erythema [MedDRA:10015150]
Periungual erythema [MedDRA:10015150]
Erythroderma (in some patients) [OMIM:Erythroderma (in some patients)]
Erythema multiforme [MedDRA:10015218]
Erythema Multiforme [Orphanet:23260]
Erythema multiforme (disorder) [Orphanet:23260]
Erythemas [MedDRA:10015151]
Dermatitis exfoliative [MedDRA:10012455]
Quality:
Cross references:
HPO:0010783 "Erythema" [Orphanet:23260]
Orphanet:23260 "Erythema/erythematous lesions/erythroderma/polymorphous erythema" [Orphanet:23260]
OMIM: "Erythroderma" [OMIM:Erythroderma]
OMIM: "Generalized erythroderma" [OMIM:Generalized erythroderma]
OMIM: "Generalized erythrodermia" [OMIM:Generalized erythrodermia]
OMIM: "Erythroderma (in some patients)" [OMIM:Erythroderma (in some patients)]
UMLS:C0041834 "Erythema" [Orphanet:23260]
UMLS:C0011606 "Exfoliative dermatitis" [Orphanet:23260]
UMLS:C0014742 "Erythema Multiforme" [Orphanet:23260]
Is a (Direct Parents):
MedDRA Exfoliative conditions
Orphanet Skin rash
MedDRA Epidermal and dermal conditions
HPO         Inflammatory abnormality of the skin
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 physiology(HPO:0011122)
                   Inflammatory abnormality of the skin(HPO:0011123)
                      Erythroderma(HPO:0001019)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Epidermal and dermal conditions(MedDRA:10014982)
       Exfoliative conditions(MedDRA:10015664)
          Erythroderma(HPO:0001019)
       Erythroderma(HPO:0001019)
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

BRESEK syndrome (Orphanet:85284)
Bathing suit ichthyosis (Orphanet:100976)
Bloom syndrome (Orphanet:125)
Congenital reticular ichthyosiform erythroderma (Orphanet:281190)
DK1-CDG (Orphanet:91131)
EPIDERMOLYTIC HYPERKERATOSIS (OMIM:113800)
Epidermolytic ichthyosis (Orphanet:312)
ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS (OMIM:242150)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5 (OMIM:604777)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 (OMIM:612281)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 7 (OMIM:615022)
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS (OMIM:602540)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome (Orphanet:37042)
MELAS (Orphanet:550)
MPDU1-CDG (Orphanet:79323)
Neonatal inflammatory skin and bowel disease (Orphanet:294023)
Netherton syndrome (Orphanet:634)
Omenn syndrome (Orphanet:39041)
Reticular dysgenesis (Orphanet:33355)
Severe dermatitis-multiple allergies-metabolic wasting syndrome (Orphanet:369992)
Stern-Lubinsky-Durrie syndrome (Orphanet:3194)
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE (OMIM:601675)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)