Heiner syndrome
Synonyms: Cow's milk-induced pulmonary hypersensitivity syndrome
- Type
- Disease
- Group
- Disorder
- Age of onset
- Infancy
- Status
- active
Heiner syndrome, also called cow's milk hypersensitivity, is a food induced pulmonary hypersensiting syndrome that affects primarily infants and that is characterized by pulmonary hemosiderosis, digestive bleeding, anemia and poor growing, improving with elimination of cow's milk from the diet.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Heiner syndrome | Cow's milk-induced pulmonary hypersensitivity syndrome |
| fr | Syndrome de Heiner | Syndrome d'hypersensibilité pulmonaire induit par le lait de vache |
| de | Heiner-Syndrom | Kuhmilch-Hypersensitivität · Kuhmilch-induziertes pulmonales Hypersensitivitätssyndrom |
| es | Síndrome de Heiner | Síndrome de hipersensibilidad pulmonar inducido por la leche de vaca |
| it | Sindrome di Heiner | |
| nl | Syndroom van Heiner | Door koemelk geïnduceerd pulmonale overgevoeligheidssyndroom |
| pt | Síndrome Heiner | Síndrome de hipersensibilidade pulmonar induzido pelo leite de vaca |
| pl | Zespół Heinera | Nadwrażliwość na krowie mleko |
| cs | Heinerův syndrom | Přecitlivělost na kravské mléko |
| uk | Синдром Гейнера | Підвищена чутливість до коровячого молока |
| zh | Heiner综合征 | 牛乳过敏症 |
| tr | Heiner sendromu | İnek sütüne aşırı duyarlılık |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | E83.1+ | NTBT | attributed | validated |
| ICD-10 | J99.8* | NTBT | attributed | validated |
| ICD-11 | CB05.5 | NTBT | index | validated |
| MONDO | 0020554 | E | validated | |
| UMLS | C3873343 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:264944Secondary interstitial lung disease in childhood and adulthood
rare respiratory diseases; rare transplant-related disorders
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | <1 / 1 000 000 | 0.07 / 100 000 | Worldwide | Value and class | 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.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/99932
- This record as JSON: /data/d/99932.json