Seborrheic dermatitis
Symptom Information:
Symptom ID: | HPO:0001051 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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) Eczema(HPO:0000964) Seborrheic dermatitis(HPO:0001051) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin appendage conditions(MedDRA:10040798) Sebaceous gland disorders(MedDRA:10039782) Seborrheic dermatitis(HPO:0001051) Epidermal and dermal conditions(MedDRA:10014982) Dermatitis and eczema(MedDRA:10012435) Seborrheic dermatitis(HPO:0001051) |
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Database Frequency: | 25 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
22q11.2 deletion syndrome | (Orphanet:567) |
3-@METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY | (OMIM:210210) |
Amelo-onycho-hypohidrotic syndrome | (Orphanet:1028) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
Biotinidase deficiency | (Orphanet:79241) |
Classical phenylketonuria | (Orphanet:79254) |
Cranio-osteoarthropathy | (Orphanet:1525) |
DERMATITIS, ATOPIC | (OMIM:603165) |
DIGEORGE SYNDROME | (OMIM:188400) |
Dubowitz syndrome | (Orphanet:235) |
Epidermodysplasia verruciformis | (Orphanet:302) |
Erythroderma desquamativum | (Orphanet:314) |
Familial benign copper deficiency | (Orphanet:1551) |
Hurler syndrome | (Orphanet:93473) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Letterer-Siwe disease | (Orphanet:99870) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 | (OMIM:611091) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Pachydermoperiostosis | (Orphanet:2796) |
Seborrhea-like dermatitis with psoriasiform elements | (Orphanet:168606) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Transketolase deficiency | (ORPHA:488618) |