ORPHA:79485

Phakomatosis spilorosea

Synonyms: Phakomatosis pigmentovascularis type 3

Orphadata ships no English definition for this code.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Phakomatosis spilorosea	Phakomatosis pigmentovascularis type 3
fr	Phacomatose spilorosea	Phacomatose pigmento-vasculaire type III
de	Phakomatosis spilorosea	Phakomatosis pigmentovascularis Typ III
es	Facomatosis spilorosea	Facomatosis pigmentovascular tipo 3
it	Facomatosi spilorosea	Facomatosi pigmento-vascolare, tipo 3
nl	Phakomatosis spilorosea	= en
pt	Facomatose spilorosea
pl	Fakomatoza barwnikowo-naczyniowa	Fakomatoza barwnikowo-naczyniowa typu 3
cs	Phakomatosis spilorosea	Phakomatosis pigmentovascularis, typ 3
uk	Факоматоз спілороза	Факоматоз пігментно-судинний, тип 3
zh	色素血管性斑痣性错构瘤病3型	色素血管性斑痣性错构瘤病3型
tr	Fakomatoz spilorosea	Fakomatoz pigmentovasküler tip 3

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	Q85.8	NTBT	attributed	validated
ICD-11	LD2D.Y	NTBT	index	validated
MONDO	0019327	E		validated
UMLS	C3839763	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

ORPHA:2875Phakomatosis pigmentovascularis
rare developmental anomalies during embryogenesis; rare genetic diseases; rare skin diseases; rare ophthalmic disorders; rare circulatory system diseases

No children.

0 direct

Orphanet records no gene directly on this code.

0 records

No prevalence record in this release.

Orphanet has no HPO annotation for this code in this release.