ORPHA:217560
Neuroendocrine cell hyperplasia of infancy
Synonyms: NCHI · NEHI
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Infancy, Neonatal
- Status
- active
Neuroendocrine cell hyperplasia of infancy (NCHI) is a non-lethal pediatric form of interstitial lung disease (ILD) characterized by tachypnea without respiratory failure.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Neuroendocrine cell hyperplasia of infancy | NCHI · NEHI |
| fr | Hyperplasie des cellules neuroendocrines du nourrisson | = en |
| de | Neuroendokrine Zellhyperplasie der Kindheit | NEHI |
| es | Hiperplasia de células neuroendocrinas del lactante | = en |
| it | Iperplasia infantile delle cellule neuroendocrine | = en |
| nl | Hyperplasie van neuro-endocriene cellen in de zuigelingentijd | = en |
| pt | Hiperplasia celular neuroendócrina da infância | |
| pl | Dziecięca hiperplazja komórek endokrynowych | = en |
| cs | Neuroendokrinní buněčná hyperplázie dětského věku | = en |
| uk | Нейроендокринна клітинна гіперплазія дитячого віку | = en |
| zh | 婴儿神经内分泌细胞增生 | = en |
| tr | Süt çocuğunda nöroendokrin hücre hiperplazisi | = en |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | J84.8 | NTBT | attributed | validated |
| ICD-11 | CB04.7 | E | specific | validated |
| MONDO | 0016322 | E | validated | |
| UMLS | C3161105 | E | validated | |
| MedDRA | 10072968 | 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:264694Interstitial lung disease specific to infancy
rare respiratory diseases; rare transplant-related disorders
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
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/217560
- This record as JSON: /data/d/217560.json