Congenital ichthyosiform erythroderma
Symptom Information:
Symptom ID: | HPO:0007431 | |||||
Synonyms: |
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Quality: | ||||||
Cross references: |
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Is a (Direct Parents): |
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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) Ichthyosis(HPO:0008064) Congenital ichthyosiform erythroderma(HPO:0007431) MedDRA: |
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Database Frequency: | 17 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Bathing suit ichthyosis | (Orphanet:100976) |
CHILD syndrome | (Orphanet:139) |
Congenital cataract - ichthyosis | (Orphanet:1376) |
Gaucher disease type 2 | (Orphanet:77260) |
Harlequin ichthyosis | (Orphanet:457) |
ICHTHYOSIS AND MALE HYPOGONADISMRUD SYNDROME, INCLUDED | (OMIM:308200) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10 | (OMIM:615024) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 | (OMIM:602400) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A | (OMIM:601277) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 9 | (OMIM:615023) |
ICHTHYOSIS, SPLIT HAIRS, AND AMINO ACIDURIA | (OMIM:242550) |
Ichthyosis-hypotrichosis syndrome | (Orphanet:91132) |
NEUTROPHIL MIGRATION | (OMIM:162820) |
SJOGREN-LARSSON-LIKE ICHTHYOSIS WITHOUT CNS OR EYE INVOLVEMENT | (OMIM:270220) |
Self-healing collodion baby | (Orphanet:281122) |
Syndromic X-linked ichthyosis | (Orphanet:281090) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |