ORPHA:202
Crandall syndrome
inactive · moved to ORPHA:123Björnstad syndrome
Synonyms: Alopecia-deafness-hypogonadism syndrome · Alopecia-hearing loss-hypogonadism syndrome · Alopecia-sensorineural deafness-hypogonadism syndrome · Alopecia-sensorineural hearing loss-hypogonadism syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Björnstad syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Crandall syndrome | Alopecia-deafness-hypogonadism syndrome · Alopecia-hearing loss-hypogonadism syndrome · Alopecia-sensorineural deafness-hypogonadism syndrome · Alopecia-sensorineural hearing loss-hypogonadism syndrome |
| fr | Syndrome de Crandall | Syndrome d'alopécie-surdité neurosensorielle-hypogonadisme · Syndrome d'alopécie-surdité-hypogonadisme |
| de | Crandall-Syndrom | Alopezie-Schwerhörigkeit-Hypogonadismus-Syndrom · Alopezie-sensorineurale Schwerhörigkeit-Hypogonadismus-Syndrom |
| es | Síndrome de Crandall | Síndrome de alopecia-hipoacusia neurosensorial-hipogonadismo · Síndrome de alopecia-hipoacusia-hipogonadismo · Síndrome de alopecia-sordera neurosensorial-hipogonadismo · Síndrome de alopecia-sordera-hipogonadismo |
| it | Sindrome di Crandall | Sindrome alopecia-sordità-ipogonadismo |
| nl | Syndroom van Crandall | Alopecie - doofheid - hypogonadisme-syndroom · Alopecie - gehoorverlies - hypogonadisme-syndroom · Alopecie - sensorineuraal gehoorverlies - hypogonadisme-syndroom · Alopecie - sensorineurale doofheid - hypogonadisme-syndroom |
| pt | Síndrome Crandall | |
| pl | Zespół Crandalla | Zespół łysienia, głuchoty i hipogonadyzmu |
| cs | Crandallův syndrom | Syndrom zahrnující alopecii, hluchotu a hypogonadismus |
| uk | Синдром Крендалла | Синдром алопеції-глухоти-гіпогонадизму · Синдром алопеції-глухоти-гіпогонадизму · Синдром алопеції-сенсоневральної глухоти-гіпогонадизму · Алопеція-сенсоневральна туговухість-гіпогонадизм |
| zh | Crandall综合征 | 脱发-感音神经性听力丧失-性腺功能减退综合征 |
| tr | Crandall sendromu | Alopesi-sağırlık-hipogonadizm sendromu · Alopesi-işitme kaybı-hipogonadizm sendromu · Alopesi-sensörinöral sağırlık-hipogonadizm sendromu · Alopesi-sensörinöral işitme kaybı-hipogonadizm sendromu |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016067 | E | validated | |
| UMLS | C0432348 | E | validated | |
| GARD | 1561 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/202
- This record as JSON: /data/d/202.json