Atopic dermatitis
Symptom Information:
Symptom ID: | HPO:0001047 | ||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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) Atopic dermatitis(HPO:0001047) MedDRA: Immune system disorders(MedDRA:10021428) Allergic conditions(MedDRA:10001708) Atopic disorders(MedDRA:10052737) Atopic dermatitis(HPO:0001047) Skin and subcutaneous tissue disorders(MedDRA:10040785) Epidermal and dermal conditions(MedDRA:10014982) Dermatitis and eczema(MedDRA:10012435) Atopic dermatitis(HPO:0001047) |
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Database Frequency: | 20 / 7739 | ||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AICARDI-GOUTIERES SYNDROME 7 | (OMIM:615846) |
ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY | (OMIM:614262) |
Autosomal recessive hyper-IgE syndrome | (Orphanet:169446) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Classical mycosis fungoides | (Orphanet:2584) |
Classical phenylketonuria | (Orphanet:79254) |
Combined immunodeficiency due to DOCK8 deficiency | (Orphanet:217390) |
DERMATITIS, ATOPIC | (OMIM:603165) |
Dubowitz syndrome | (Orphanet:235) |
IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTIONAND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST | (OMIM:146840) |
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | (Orphanet:37042) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 | (OMIM:611091) |
MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM | (OMIM:606242) |
MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES | (OMIM:606772) |
Maternal hyperphenylalaninemia | (Orphanet:2209) |
Monosomy 18q | (Orphanet:1600) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |