Prepubertal anorexia nervosa
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
A rare neurologic disease with psychiatric involvement characterized by significantly lower-than-expected body weight due to voluntary reduction of food intake, intense fear of becoming overweight, and a distorted body image, in prepubescent children. Secondary manifestations include growth, developmental, and pubertal delay, decreased bone density, severe metabolic and endocrine dysfunction, cognitive impairment, depression, deterioration of academic or athletic performance, as well as difficulties in familial and peer relations, among others.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Prepubertal anorexia nervosa | |
| fr | Anorexie mentale de l'enfant | |
| de | Anorexia nervosa, präpubertäre | |
| es | Anorexia nerviosa prepuberal | |
| it | Anoressia nervosa prepuberale | |
| nl | Prepuberale anorexia nervosa | |
| pt | Anorexia nervosa pré-pubertária | |
| pl | Jadłowstręt psychiczny w okresie przedpokwitaniowym/anorexia nervosa w okresie przedpokwitaniowym | |
| cs | Předpubertální mentální anorexie | |
| uk | Нервова анорексія в препубертатному віці | |
| zh | 青春期前神经性厌食 | |
| tr | Prepubertal anoreksiya nervoza |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | F50.0 | NTBT | attributed | validated |
| MONDO | 0033926 | E | validated | |
| UMLS | C5568567 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:181384Rare hypothalamic or pituitary disease
rare endocrine diseases - ORPHA:98033Rare neurologic disease with psychiatric involvement
rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/525738
- This record as JSON: /data/d/525738.json