Acne

Symptom Information:

Symptom ID: HPO:0001061
Synonyms:
Acne (disorder) [Orphanet:23410]
Acne [Orphanet:23410]
Acne [OMIM:Acne]
Acne/acnea [Orphanet:23410]
Acne [MedDRA:10000496]
Acne aggravated [MedDRA:10000496]
Acne comedonal [MedDRA:10000496]
Acne follicular [MedDRA:10000496]
Acne follicular papular pustular etc [MedDRA:10000496]
Acne medicamentosa [MedDRA:10000496]
Acne NOS [MedDRA:10000496]
Acne papular [MedDRA:10000496]
Acne steroid [MedDRA:10000496]
Acne steroid-induced [MedDRA:10000496]
Acne vulgaris [MedDRA:10000496]
Blackheads [MedDRA:10000496]
Comedo [MedDRA:10000496]
Comedome [MedDRA:10000496]
Comedone [MedDRA:10000496]
Exacerbation of acne [MedDRA:10000496]
Other acne [MedDRA:10000496]
Pimple [MedDRA:10000496]
Pimples [MedDRA:10000496]
Steroid acne [MedDRA:10000496]
Acne follicular papular pustular etc. [MedDRA:10000496]
Comedones [OMIM:Comedones]
Acnes [MedDRA:10000497]
Quality:
Cross references:
Orphanet:23410 "Acne/acnea" [Orphanet:23410]
OMIM: "Acne" [OMIM:Acne]
OMIM: "Comedones" [OMIM:Comedones]
UMLS:C0702166 "Acne" [HPO:0001061]
UMLS:C0702166 "Acne" [Orphanet:23410]
Is a (Direct Parents):
HPO         Comodogenic acne
Orphanet Abnormality of the skin
MedDRA Skin appendage conditions
HPO         Acne inversa
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)
                      Acne(HPO:0001061)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin appendage conditions(MedDRA:10040798)
       Acne(HPO:0001061)
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)