ORPHA:98027
Rare disease with odontological manifestation
- 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 disease with odontological manifestation | |
| fr | Maladie rare avec atteinte odontologique | |
| de | Odontologische Manifestation, seltener Krankheit mit | |
| es | Enfermedad rara con manifestación odontológica | |
| it | Malattia rara con manifestazione odontologica | |
| nl | Zeldzame ziekte met odontologische manifestatie | |
| pt | Doença rara com manifestações odontológicas | |
| pl | Rzadkie choroby z objawami stomatologicznymi | |
| cs | Vzácná onemocnění s odontologickou manifestací | |
| uk | Рідкісне захворювання з одонтологічним проявом | |
| zh | 伴口腔累及的罕见疾病 | |
| tr | Odontolojik belirtili nadir hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681548 | 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:98026Rare odontologic disease
rare odontological diseases
Children (30):
- ORPHA:247676Adult hypophosphatasia
- ORPHA:65282Carvajal syndrome
- ORPHA:184Cherubism
- ORPHA:247667Childhood-onset hypophosphatasia
- ORPHA:99792Dentin dysplasia-sclerotic bones syndrome
- ORPHA:708036Ectodermal dysplasia with agenesis of maxillary lateral incisors and mandibular anterior teeth
- ORPHA:708043Ectodermal dysplasia with oligodontia-hand and foot malformation-hypoplastic nipples
- ORPHA:2325Epidermolysis bullosa simplex with anodontia/hypodontia
- ORPHA:476096Erythrokeratodermia-cardiomyopathy syndrome
- ORPHA:714399Global developmental delay-dental enamel defects-ataxia syndrome
- ORPHA:377Gorlin syndrome
- ORPHA:685067Hypodontia-scalp hypotrichosis-facial dysmorphism syndrome
- ORPHA:363523Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome
- ORPHA:238468Hypohidrotic ectodermal dysplasia
- ORPHA:98813Hypohidrotic ectodermal dysplasia with immunodeficiency
- ORPHA:464Incontinentia pigmenti
- ORPHA:247651Infantile hypophosphatasia
- ORPHA:79402Intermediate generalized junctional epidermolysis bullosa
- ORPHA:79405Junctional epidermolysis bullosa inversa
- ORPHA:79403Junctional epidermolysis bullosa with pyloric atresia
- ORPHA:2407Laryngo-onycho-cutaneous syndrome
- ORPHA:79406Late-onset junctional epidermolysis bullosa
- ORPHA:231556Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome
- ORPHA:251393Localized junctional epidermolysis bullosa
- ORPHA:557003Oculoskeletodental syndrome
- ORPHA:247685Odontohypophosphatasia
- ORPHA:75392Periodontal Ehlers-Danlos syndrome
- ORPHA:447961Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome
- ORPHA:167762Rare disease with dentinogenesis imperfecta
- ORPHA:79404Severe generalized junctional epidermolysis bullosa
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/98027
- This record as JSON: /data/d/98027.json