ORPHA:93460
Overgrowth syndrome
- 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 | Overgrowth syndrome | |
| fr | Syndrome avec croissance excessive | |
| de | Großwuchs-Syndrom | |
| es | Síndrome de sobrecrecimiento | |
| it | Sindrome da gigantismo | |
| nl | Overgroeisyndroom | |
| pt | Síndrome de sobrecrescimento | |
| pl | Zespół nadmiernego wzrostu | |
| cs | Syndromy nadměrného vzrůstu | |
| uk | Синдром надмірного росту | |
| zh | 过度生长综合征 | |
| tr | Aşırı büyüme sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q87.3 | E | specific | validated |
| ICD-11 | LD2C | E | specific | validated |
| MONDO | 0019716 | E | validated | |
| UMLS | C2986703 | E | validated | |
| MedDRA | 10088693 | 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:183573Genetic overgrowth/obesity syndrome
rare genetic diseases - ORPHA:139024Overgrowth/obesity syndrome
rare developmental anomalies during embryogenesis
Children (29):
- ORPHA:30030511p15.4 microduplication syndrome
- ORPHA:109Bannayan-Riley-Ruvalcaba syndrome
- ORPHA:116Beckwith-Wiedemann syndrome
- ORPHA:642675CHD8 overgrowth syndrome
- ORPHA:93461Chromosomal disease with overgrowth
- ORPHA:1926Diabetic embryopathy
- ORPHA:714737Diffuse capillary malformation with overgrowth
- ORPHA:404476Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome
- ORPHA:293964Hypoinsulinemic hypoglycemia and body hemihypertrophy
- ORPHA:2128Isolated hemihyperplasia
- ORPHA:597738Luscan-Lumish syndrome
- ORPHA:163634Maffucci syndrome
- ORPHA:420179Malan overgrowth syndrome
- ORPHA:561Marshall-Smith syndrome
- ORPHA:457359Megalencephaly-severe kyphoscoliosis-overgrowth syndrome
- ORPHA:33445Neuroectodermal melanolysosomal disease
- ORPHA:296Ollier disease
- ORPHA:137634Overgrowth-macrocephaly-facial dysmorphism syndrome
- ORPHA:530313PIK3CA-related overgrowth spectrum disorder
- ORPHA:659387PRC-2 complex-related overgrowth spectrum
- ORPHA:726807PTEN hamartoma of soft tissue
- ORPHA:90307Parkes Weber syndrome
- ORPHA:2849Perlman syndrome
- ORPHA:744Proteus syndrome
- ORPHA:137608Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome
- ORPHA:373Simpson-Golabi-Behmel syndrome
- ORPHA:821Sotos syndrome
- ORPHA:3205Sturge-Weber syndrome
- ORPHA:404443Tatton-Brown-Rahman 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/93460
- This record as JSON: /data/d/93460.json