Eczematoid dermatitis
Symptom Information:
Symptom ID: | HPO:0000976 | |||||||||||||||||||||||||||||||||||
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 physiology(HPO:0011122) Inflammatory abnormality of the skin(HPO:0011123) Eczema(HPO:0000964) Eczematoid dermatitis(HPO:0000976) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Epidermal and dermal conditions(MedDRA:10014982) Dermatitis and eczema(MedDRA:10012435) Eczematoid dermatitis(HPO:0000976) |
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Database Frequency: | 22 / 7739 | |||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
Classical mycosis fungoides | (Orphanet:2584) |
Classical phenylketonuria | (Orphanet:79254) |
Combined immunodeficiency due to ZAP70 deficiency | (Orphanet:911) |
Cranio-osteoarthropathy | (Orphanet:1525) |
DERMATITIS, ATOPIC | (OMIM:603165) |
Dubowitz syndrome | (Orphanet:235) |
EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED | (OMIM:130090) |
Extramammary Paget disease | (Orphanet:2800) |
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE | (OMIM:233690) |
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE I | (OMIM:233700) |
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE II | (OMIM:233710) |
GRANULOMATOUS DISEASE, CHRONIC, X-LINKED | (OMIM:306400) |
ICHTHYOSIS VULGARIS | (OMIM:146700) |
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | (Orphanet:37042) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 | (OMIM:611091) |
Maternal hyperphenylalaninemia | (Orphanet:2209) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Thymic aplasia | (Orphanet:83471) |