Atopic dermatitis

Symptom Information:

Symptom ID: HPO:0001047
Synonyms:
Atopic dermatitis, chronic [HPO:0001047]
Dermatitis, Atopic [HPO:0001047]
Eczema [Orphanet:23230]
Eczema (disorder) [Orphanet:23230]
Atopic dermatitis [OMIM:Atopic dermatitis]
Atopic dermatitis, chronic [OMIM:Atopic dermatitis, chronic]
Eczema [MedDRA:10014184]
Dermatitis eczematoid [MedDRA:10014184]
Eczema (rash) in the outer ear [MedDRA:10014184]
Eczema acute [MedDRA:10014184]
Eczema aggravated [MedDRA:10014184]
Eczema exacerbated [MedDRA:10014184]
Eczema facial [MedDRA:10014184]
Eczema NOS [MedDRA:10014184]
Eczema of external auditory meatus [MedDRA:10014184]
Eczema papular [MedDRA:10014184]
Eczematous dermatitis [MedDRA:10014184]
Eczematous nipple [MedDRA:10014184]
Eczematous rash [MedDRA:10014184]
Erythematosquamous dermatosis [MedDRA:10014184]
Generalised eczematous reaction [MedDRA:10014184]
Other erythematosquamous dermatosis [MedDRA:10014184]
Reaction eczematous [MedDRA:10014184]
Scrotal eczema [MedDRA:10014184]
Generalized eczematous reaction [MedDRA:10014184]
Epiderma spongiosis [MedDRA:10014184]
Vulval eczema [MedDRA:10014184]
Chronic eczema [MedDRA:10014184]
Acute spongiotic dermatitis [MedDRA:10014184]
Subacute spongiotic dermatitis [MedDRA:10014184]
Eczema (8 of 23) [OMIM:Eczema (8 of 23)]
Eczema (face and flexural areas) [OMIM:Eczema (face and flexural areas)]
Eczema (in 1 patient) [OMIM:Eczema (in 1 patient)]
Eczema (in some patients) [OMIM:Eczema (in some patients)]
Eczema (perifollicular accentuation) [OMIM:Eczema (perifollicular accentuation)]
Eczema (rare) [OMIM:Eczema (rare)]
Eczematous dermatitis [OMIM:Eczematous dermatitis]
Dermatitis atopic [MedDRA:10012438]
Quality:
Cross references:
HPO:0000964 "Eczema" [Orphanet:23230]
HPO:0000976 "Eczematoid dermatitis" [Orphanet:23230]
Orphanet:23230 "Eczema" [Orphanet:23230]
OMIM: "Atopic dermatitis" [OMIM:Atopic dermatitis]
OMIM: "Atopic dermatitis, chronic" [OMIM:Atopic dermatitis, chronic]
OMIM: "Eczema (8 of 23)" [OMIM:Eczema (8 of 23)]
OMIM: "Eczema (face and flexural areas)" [OMIM:Eczema (face and flexural areas)]
OMIM: "Eczema (in 1 patient)" [OMIM:Eczema (in 1 patient)]
OMIM: "Eczema (in some patients)" [OMIM:Eczema (in some patients)]
OMIM: "Eczema (perifollicular accentuation)" [OMIM:Eczema (perifollicular accentuation)]
OMIM: "Eczema (rare)" [OMIM:Eczema (rare)]
OMIM: "Eczematous dermatitis" [OMIM:Eczematous dermatitis]
UMLS:C0013595 "Eczema" [Orphanet:23230]
Is a (Direct Parents):
MedDRA Atopic disorders
Orphanet Skin rash
MedDRA Dermatitis and eczema
HPO         Inflammatory abnormality of the skin
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)
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)