Acne
Symptom Information:
Symptom ID: | HPO:0001061 | |||||||||||||||||||||||||||
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) Acne(HPO:0001061) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin appendage conditions(MedDRA:10040798) Acne(HPO:0001061) |
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Database Frequency: | 33 / 7739 | |||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
15q14 microdeletion syndrome | (Orphanet:261190) |
22q11.2 deletion syndrome | (Orphanet:567) |
ACTH-dependent Cushing syndrome | (Orphanet:99892) |
ACTH-independent Cushing syndrome | (Orphanet:99893) |
Acromegaly | (Orphanet:963) |
Apert syndrome | (Orphanet:87) |
Aspartylglucosaminuria | (Orphanet:93) |
Atypical Mayer-Rokitansky-Küster-Hauser syndrome | (Orphanet:247768) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
Behçet disease | (Orphanet:117) |
Chronic recurrent multifocal osteomyelitis | (Orphanet:324964) |
Cortisone reductase deficiency 1 | (OMIM:604931) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Cushing syndrome due to ectopic ACTH secretion | (Orphanet:99889) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
Familial benign copper deficiency | (Orphanet:1551) |
Hyperandrogenism due to cortisone reductase deficiency | (Orphanet:168588) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Lipoid proteinosis | (Orphanet:530) |
Majeed syndrome | (Orphanet:77297) |
Mucolipidosis type 3 | (Orphanet:577) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4 | (OMIM:615830) |
Pachydermoperiostosis | (Orphanet:2796) |
Polycystic ovaries - urethral sphincter dysfunction | (Orphanet:2795) |
Pseudoxanthoma elasticum | (Orphanet:758) |
Pyogenic arthritis - pyoderma gangrenosum - acne | (Orphanet:69126) |
Rhizomelic syndrome, Urbach type | (Orphanet:3098) |
SAPHO syndrome | (Orphanet:793) |
Spondyloepimetaphyseal dysplasia, Pakistani type | (Orphanet:93282) |
Subaortic stenosis - short stature | (Orphanet:3191) |
Testotoxicosis | (Orphanet:3000) |
W syndrome | (Orphanet:2804) |