ORPHA:240371
Syndromic obesity
- 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 | Syndromic obesity | |
| fr | Obésité syndromique | |
| de | Adipositas, syndromale | |
| es | Obesidad sindrómica | |
| it | Obesità sindromica | |
| nl | Syndromale obesitas | |
| pt | Obesidade sindromática | |
| pl | Otyłość syndromiczna | |
| cs | Syndromická obezita | |
| uk | Синдромальне ожиріння | |
| zh | 综合征性肥胖 | |
| tr | Sendromik obezite |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16565 | E | validated | |
| UMLS | C5680938 | 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 (2):
- ORPHA:77828Genetic obesity
rare genetic diseases; rare endocrine diseases - ORPHA:139024Overgrowth/obesity syndrome
rare developmental anomalies during embryogenesis
Children (39):
- ORPHA:64Alström syndrome
- ORPHA:110Bardet-Biedl syndrome
- ORPHA:127Borjeson-Forssman-Lehmann syndrome
- ORPHA:65759Carpenter syndrome
- ORPHA:600731Clark-Baraitser syndrome
- ORPHA:192Coffin-Lowry syndrome
- ORPHA:444077Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome
- ORPHA:193Cohen syndrome
- ORPHA:363741Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome
- ORPHA:652487Developmental delay-overweight-facial dysmorphism-behavioral abnormalities syndrome
- ORPHA:261222Distal 16p11.2 microdeletion syndrome
- ORPHA:99704Early-onset obesity-hyperphagia-severe developmental delay syndrome
- ORPHA:908Fragile X syndrome
- ORPHA:2183Hydrocephalus-obesity-hypogonadism syndrome
- ORPHA:352530Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome
- ORPHA:397973Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome
- ORPHA:369950Intellectual disability-seizures-macrocephaly-obesity syndrome
- ORPHA:85282MEHMO syndrome
- ORPHA:2563MOMO syndrome
- ORPHA:75858MORM syndrome
- ORPHA:647799MYT1L-related developmental delay-intellectual disability-obesity syndrome
- ORPHA:2637Microcephalic osteodysplastic primordial dwarfism type II
- ORPHA:589905PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome
- ORPHA:739Prader-Willi syndrome
- ORPHA:398073Prader-Willi-like syndrome
- ORPHA:620363Primary hypomagnesemia-generalized seizures-intellectual disability-obesity syndrome
- ORPHA:79443Pseudohypoparathyroidism type 1A
- ORPHA:79444Pseudohypoparathyroidism type 1C
- ORPHA:79445Pseudopseudohypoparathyroidism
- ORPHA:293987Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome
- ORPHA:783Rubinstein-Taybi syndrome
- ORPHA:464288Short stature-brachydactyly-obesity-global developmental delay syndrome
- ORPHA:819Smith-Magenis syndrome
- ORPHA:521390Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome
- ORPHA:276630Symptomatic form of Coffin-Lowry syndrome in female carriers
- ORPHA:254516Temple syndrome
- ORPHA:893WAGR syndrome
- ORPHA:3459Wilson-Turner syndrome
- ORPHA:1435Xq21 microdeletion 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/240371
- This record as JSON: /data/d/240371.json