Erythroderma
Symptom Information:
Symptom ID: | HPO:0001019 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||
Quality: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||
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) |