ORPHA:168621
Dysplasia of head of femur, Meyer type
Synonyms: DECF · Dysplasia epiphysealis capitis femoris · Meyer dysplasia
- Type
- Disease
- Group
- Disorder
- Age of onset
- Infancy, Neonatal
- Status
- active
Meyer dysplasia of the femoral head is a mild localized form of skeletal dysplasia characterized by delayed, irregular ossification of femoral capital epiphysis.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Dysplasia of head of femur, Meyer type | DECF · Dysplasia epiphysealis capitis femoris · Meyer dysplasia |
| fr | Dysplasie de la tête du fémur type Meyer | Dysplasie de Meyer · Dysplasie épiphysaire de la tête du fémur |
| de | Femurkopfdysplasie Typ Meyer | DECF · Dysplasia epiphysealis capitis femoris |
| es | Displasia de la cabeza femoral tipo Meyer | Displasia de Meyer · Displasia epifisaria de la cabeza femoral |
| it | Displasia della testa del femore, tipo Meyer | DECF · Displasia di Meyer · Displasia epifisaria della testa del femore |
| nl | Dysplasie van femurkop, Meyer-type | DECF · Dysplasia epiphysealis capitis femoris · Dysplasie, Meyer-type |
| pt | Displasia da cabeça do femur, tipo Meyer | DECF · Displasia Meyer · Displasia epiphysealis capitis femoris |
| pl | Dysplazja głowy kości udowej, typ Meyera | = en |
| cs | Dysplázie hlavice femuru, Meyerův typ | = en |
| uk | Дисплазія головки стегнової кістки, тип Мейєра | DECF · Дисплазія епіфізарного відростка стегнової кістки · Дисплазія Мейєра |
| zh | Meyer型股骨头发育不良 | 股骨头骨骺发育不良 |
| tr | Femur başı displazisi, Meyer tipi | Meyer displazisi · Displazi epiphysealis capitis femoris |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q78.8 | NTBT | attributed | validated |
| ICD-11 | LD24.6Y | NTBT | index | validated |
| MONDO | 0015678 | E | validated | |
| UMLS | C4274970 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:93419Rare bone disease
rare bone diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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HPO phenotypes
13 annotations · validated 2021-11-30| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Frequent (79-30%) | ||
| HP:0008829 | Delayed femoral head ossification | |
| HP:0002750 | Delayed skeletal maturation | |
| HP:0008835 | Multicentric femoral head ossification | |
| Occasional (29-5%) | ||
| HP:0031955 | Antalgic gait | |
| HP:0003565 | Elevated erythrocyte sedimentation rate | |
| HP:0001974 | Increased total leukocyte count | |
| HP:0008800 | Limited hip movement | |
| HP:0012514 | Lower limb pain | |
| HP:0002515 | Waddling gait | |
| Very rare (<4-1%) | ||
| HP:0001374 | Congenital hip dislocation | |
| HP:0030812 | Enlarged tonsils | |
| HP:0001945 | Fever | |
| HP:0008812 | Flattened femoral head | |
Annotation source: 10482209[PMID]_21138215[PMID]
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/168621
- This record as JSON: /data/d/168621.json