ORPHA:79364
Alopecia
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Alopecia | |
| fr | Alopécie | |
| de | Alopezie | |
| es | Alopecia | |
| it | Alopecia | |
| nl | Alopecie | Alopecia · Haaruitval · Kaalheid |
| pt | Alopecia | |
| pl | Łysienie | |
| cs | Alopecie | |
| uk | Алопеція | |
| zh | 秃头 | |
| tr | Alopesi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | ED70 | E | specific | validated |
| MONDO | 0004907 | E | validated | |
| MONDO | 4907 | E | validated | |
| MeSH | D000505 | E | validated | |
| UMLS | C0002170 | E | validated | |
| MedDRA | 10001760 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:79363Hair anomaly
rare skin diseases
Children (27):
- ORPHA:157954ANE syndrome
- ORPHA:1006Alopecia antibody deficiency
- ORPHA:700Alopecia totalis
- ORPHA:701Alopecia universalis
- ORPHA:1008Alopecia-epilepsy-pyorrhea-intellectual disability syndrome
- ORPHA:2850Alopecia-intellectual disability syndrome
- ORPHA:1014Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome
- ORPHA:86819Atrichia with papular lesions
- ORPHA:729781Congenital generalized alopecia-hypoplastic kidneys-facial dysmorphism-sensorineural deafness syndrome
- ORPHA:254492Frontal fibrosing alopecia
- ORPHA:228390Frontonasal dysplasia-alopecia-genital anomalies syndrome
- ORPHA:505Graham Little-Piccardi-Lassueur syndrome
- ORPHA:217407Hereditary hypotrichosis with recurrent skin vesicles
- ORPHA:55654Hypotrichosis simplex
- ORPHA:90368Hypotrichosis simplex of the scalp
- ORPHA:330029Hypotrichosis-deafness syndrome
- ORPHA:2273Ichthyosis follicularis-alopecia-photophobia syndrome
- ORPHA:91132Ichthyosis-hypotrichosis syndrome
- ORPHA:525Lichen planopilaris
- ORPHA:168Loose anagen syndrome
- ORPHA:443995Mandibulofacial dysostosis with alopecia
- ORPHA:444Marie Unna hereditary hypotrichosis
- ORPHA:2701Noonan syndrome-like disorder with loose anagen hair
- ORPHA:447961Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome
- ORPHA:129Pseudopelade of Brocq
- ORPHA:346Quinquaud folliculitis decalvans
- ORPHA:3130Satoyoshi syndrome
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/79364
- This record as JSON: /data/d/79364.json