Congenital nonbullous ichthyosiform erythroderma
Symptom Information:
Symptom ID: | HPO:0007479 | |||||||||||||
Synonyms: |
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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) Congenital nonbullous ichthyosiform erythroderma(HPO:0007479) MedDRA: Pregnancy, puerperium and perinatal conditions(MedDRA:10036585) Neonatal and perinatal conditions(MedDRA:10028920) Newborn complications NEC(MedDRA:10010168) Congenital nonbullous ichthyosiform erythroderma(HPO:0007479) |
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Database Frequency: | 13 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
Dorfman-Chanarin disease | (Orphanet:98907) |
Fetal Gaucher disease | (Orphanet:85212) |
Gaucher disease type 2 | (Orphanet:77260) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3 | (OMIM:606545) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5 | (OMIM:604777) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 | (OMIM:612281) |
Ichthyosis - intellectual deficit - dwarfism - renal impairment | (Orphanet:2278) |
KETOADIPICACIDURIA | (OMIM:245130) |
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome | (Orphanet:281201) |
Lamellar ichthyosis | (Orphanet:313) |
Netherton syndrome | (Orphanet:634) |
Self-healing collodion baby | (Orphanet:281122) |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE | (OMIM:601675) |