Eczema
Symptom Information:
Symptom ID: | HPO:0000964 | |||||||||||||||||||||||||||||||||||||
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) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Epidermal and dermal conditions(MedDRA:10014982) Dermatitis and eczema(MedDRA:10012435) Eczema(HPO:0000964) |
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Database Frequency: | 81 / 7739 | |||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
2q37 microdeletion syndrome | (Orphanet:1001) |
8q21.11 microdeletion syndrome | (Orphanet:284160) |
ADULT syndrome | (Orphanet:978) |
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET | (OMIM:615952) |
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V | (OMIM:616100) |
Autoimmune lymphoproliferative syndrome with recurrent infections | (Orphanet:275517) |
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Autosomal dominant hypocalcemia | (Orphanet:428) |
Autosomal dominant hypohidrotic ectodermal dysplasia | (Orphanet:1810) |
Autosomal recessive hyper-IgE syndrome | (Orphanet:169446) |
Barth syndrome | (Orphanet:111) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
Blau syndrome | (Orphanet:90340) |
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency | (Orphanet:329255) |
Bullous pemphigoid | (Orphanet:703) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
Cataract - deafness - hypogonadism | (Orphanet:1383) |
Chronic granulomatous disease | (Orphanet:379) |
Classical mycosis fungoides | (Orphanet:2584) |
Classical phenylketonuria | (Orphanet:79254) |
Combined immunodeficiency due to DOCK8 deficiency | (Orphanet:217390) |
Cranio-osteoarthropathy | (Orphanet:1525) |
Cutis laxa | (Orphanet:209) |
DERMATITIS, ATOPIC | (OMIM:603165) |
Dermatitis herpetiformis | (Orphanet:1656) |
Dubowitz syndrome | (Orphanet:235) |
Dystrophic epidermolysis bullosa | (Orphanet:303) |
Ectodermal dysplasia syndrome | (Orphanet:79373) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Epidermolytic palmoplantar keratoderma | (Orphanet:2199) |
Erythropoietic protoporphyria | (Orphanet:79278) |
Fukuda-Miyanomae-Nakata syndrome | (Orphanet:2060) |
Grubben-de Cock-Borghgraef syndrome | (Orphanet:2101) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
Hypohidrotic ectodermal dysplasia | (Orphanet:238468) |
IMMUNODEFICIENCY 17 | (OMIM:615607) |
IMMUNODEFICIENCY 23 | (OMIM:615816) |
IMMUNODEFICIENCY 31C | (OMIM:614162) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
IgE RESPONSIVENESS, ATOPIC | (OMIM:147050) |
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | (Orphanet:37042) |
Immunodeficiency due to CD25 deficiency | (Orphanet:169100) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Intellectual deficit, X-linked - short stature - obesity | (Orphanet:3055) |
Isolated sulfite oxidase deficiency | (Orphanet:99731) |
Jacobsen syndrome | (Orphanet:2308) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Koolen-De Vries syndrome | (Orphanet:96169) |
LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA | (OMIM:608809) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 | (OMIM:611091) |
MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUALAPPEARANCE | (OMIM:612947) |
Maternal hyperphenylalaninemia | (Orphanet:2209) |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C | (OMIM:613216) |
Netherton syndrome | (Orphanet:634) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
PELGER-HUET ANOMALY | (OMIM:169400) |
POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY | (OMIM:615895) |
Phenylketonuria | (Orphanet:716) |
Pityriasis rubra pilaris | (Orphanet:2897) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Polyglucosan body myopathy type 1 | (ORPHA:397937) |
Porphyria cutanea tarda | (Orphanet:101330) |
Propionic acidemia | (Orphanet:35) |
Roifman syndrome | (Orphanet:353298) |
SENER SYNDROME | (OMIM:606156) |
SRD5A3-CDG | (Orphanet:324737) |
Say-Barber-Miller syndrome | (Orphanet:3132) |
Shwachman-Diamond syndrome | (Orphanet:811) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
T-B+ severe combined immunodeficiency due to CD45 deficiency | (Orphanet:169157) |
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency | (Orphanet:169154) |
TRICHORRHEXIS NODOSA SYNDROME | (OMIM:275550) |
W syndrome | (Orphanet:2804) |
WISKOTT-ALDRICH SYNDROME | (OMIM:277970) |
WISKOTT-ALDRICH SYNDROME | (OMIM:301000) |
WISKOTT-ALDRICH SYNDROME 2 | (OMIM:614493) |
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM | (OMIM:600903) |
Wiskott-Aldrich syndrome | (Orphanet:906) |
X-linked hypohidrotic ectodermal dysplasia | (Orphanet:181) |
X-linked thrombocytopenia with normal platelets | (Orphanet:852) |
ZINC DEFICIENCY, TRANSIENT NEONATAL | (OMIM:608118) |