ORPHA:98033
Rare neurologic disease with psychiatric involvement
- 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 | Rare neurologic disease with psychiatric involvement | |
| fr | Maladie neurologique rare avec atteinte psychiatrique | |
| de | Psychiatrische Krankheit, seltene | |
| es | Enfermedad neurológica rara con afectación psiquiátrica | |
| it | Malattia neurologica rara con coinvolgimento psichiatrico | |
| nl | Zeldzame neurologische ziekte met psychiatrische betrokkenheid | |
| pt | Doença psiquiátrica rara | |
| pl | Rzadkie choroby neurologiczne z zaburzeniami psychicznymi | |
| cs | Vzácná neurologická onemocnění s psychiatrickým postižením | |
| uk | Рідкісне неврологічне захворювання з психіатричними проявами | |
| zh | 伴精神异常的罕见神经疾病 | |
| tr | Psikiyatrik tutulum ile seyreden nadir nörolojik hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681544 | 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:98006Rare neurologic disease
rare neurological diseases
Children (20):
- ORPHA:19931815q13.3 microdeletion syndrome
- ORPHA:56722q11.2 deletion syndrome
- ORPHA:72Angelman syndrome
- ORPHA:420789Autoimmune encephalopathy with parasomnia and obstructive sleep apnea
- ORPHA:623789Body integrity dysphoria
- ORPHA:641496Childhood-onset schizophrenia
- ORPHA:648919Idiopathic catatonia
- ORPHA:157823Klüver-Bucy syndrome
- ORPHA:647799MYT1L-related developmental delay-intellectual disability-obesity syndrome
- ORPHA:589905PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome
- ORPHA:443173Postpartum psychosis
- ORPHA:739Prader-Willi syndrome
- ORPHA:398073Prader-Willi-like syndrome
- ORPHA:525738Prepubertal anorexia nervosa
- ORPHA:89043Rare dementia
- ORPHA:168778Rare pervasive developmental disorder
- ORPHA:273Steinert myotonic dystrophy
- ORPHA:83601Steroid-responsive encephalopathy associated with autoimmune thyroiditis
- ORPHA:904Williams syndrome
- ORPHA:905Wilson disease
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/98033
- This record as JSON: /data/d/98033.json