ORPHA:90395
Papular mucinosis of infancy
Synonyms: Cutaneous mucinosis of infancy
- Type
- Disease
- Group
- Disorder
- Status
- active
Papular mucinosis of infancy is a rare pediatric non progressive form of localized lichen myxedematosus characterized by the development of firm opalescent mucinous papules on the upper arms and the trunk.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Papular mucinosis of infancy | Cutaneous mucinosis of infancy |
| fr | Mucinose cutanée infantile | Mucinose papuleuse infantile |
| de | Muzinose, papulöse, des Säuglingsalters | Kutane Muzinose des Kindes |
| es | Mucinosis papular infantil | Mucinosis cutánea infantil |
| it | Mucinosi papulosa dell'infanzia | Mucinosi cutanea dell'infanzia |
| nl | Papulaire mucinose in de zuigelingentijd | Cutane mucinose in de zuigelingentijd |
| pt | Mucinose papular do lactente | |
| pl | Dziecięca mucynoza grudkowa | Dziecięca mucynoza skórna |
| cs | Papulární mucinóza kojenců | Kožní mucinóza kojenců |
| uk | Папульозний муциноз немовлят | Шкірний муциноз немовлят |
| zh | 婴儿丘疹性粘蛋白病 | 婴儿皮肤粘蛋白病 |
| tr | Süt çocuğunda papüler müsinoz | Bebeklik döneminde kutanöz müsinoz |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | L98.5 | NTBT | attributed | validated |
| ICD-11 | EB90.11 | NTBT | attributed | validated |
| MONDO | 0019580 | E | validated | |
| UMLS | C4273966 | 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:86795Localized lichen myxedematosus
rare skin diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 14 cases | Worldwide | Case(s) | Validated | 30677812[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 30677812[PMID]_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/90395
- This record as JSON: /data/d/90395.json