About: Rombo syndrome

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Rombo syndrome is characterized by vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, peripheral vasodilation with cyanosis and basal cell carcinomas

Attributes	Values
rdf:type	Item
description	Rombo syndrome is characterized by vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, peripheral vasodilation with cyanosis and basal cell carcinomas (en) angeborene Genodermatose (de)
exact match	wds:Q7362935-A942FC45-B32F-4587-9E17-0BAEBBE74FF5
exact match	http://www.orpha.net/ORDO/Orphanet_3110
Mondo ID	wds:Q7362935-536E599B-BFE1-4DF9-89C0-36566BAF45A0
DiseasesDB	wds:q7362935-C3A229A3-13BD-459E-9AB9-F18C49E5C28D
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0008390
Mondo ID	MONDO_0008390
DiseasesDB	33487
rdfs:label	Rombo syndrome (en) Rombo-Syndrom (de) syndrome de Rombo (fr)
skos:prefLabel	Rombo syndrome (en) Rombo-Syndrom (de) syndrome de Rombo (fr)
name	Rombo syndrome (en) Rombo-Syndrom (de) syndrome de Rombo (fr)
instance of	wds:Q7362935-60E79FC8-45E0-40F2-91FE-23FC85F1B52F
instance of	class of disease
subclass of	wds:Q7362935-2c32f15f-433e-b304-3499-71ec7faa9337 wds:Q7362935-390f4ffa-40e3-8327-3acd-fffb2297314c wds:Q7362935-E5DFBC92-6576-41F5-A8E3-DCE90BC3C534 wds:Q7362935-d874e343-4aa4-9272-19cc-77e2d2024f1d
subclass of	hypotrichosis basal-cell carcinoma atrophodermia vermiculata skin tumor or hamartoma
Orphanet ID	wds:Q7362935-a74d8fec-4eab-e28a-e1ba-974b82c2ce51
ICD-10-CM	wds:Q7362935-E45C1452-405C-496F-B11B-8BBDAAF1FE57
GARD rare disease ID	wds:Q7362935-96A11CCC-0B7A-4CBE-B81B-EAB4BB456CD4
OMIM ID	wds:q7362935-9FF4CDE8-4097-489A-968D-4F31B37F1D05
Orphanet ID	3110
ICD-10-CM	L98.8
GARD rare disease ID	4738
OMIM ID	180730
skos:altLabel	ROMBO SYNDROME (en) Vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, basal cell carcinomas and peripheral vasodilation with cyanosis (en)
UMLS CUI	wds:Q7362935-210AC0BA-EBD4-4F64-A78C-A1CDB8BC5475
MeSH descriptor ID	wds:Q7362935-94d41180-4ca6-a408-144c-15ea2dcfc666
Microsoft Academic ID	wds:Q7362935-E57ACF61-250C-427E-AEC2-EA6B63288272
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/C535870
Microsoft Academic ID	https://makg.org/entity/2778057327
UMLS CUI	C1867147
MeSH descriptor ID	C535870
Microsoft Academic ID	2778057327
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q7362935 Rombo syndrome https://de.wikipedia.org/wiki/Rombo-Syndrom
is main subject of	The Rombo syndrome: a familial disorder with vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, basal cell carcinomas and peripheral vasodilation with cyanosis A case of Rombo syndrome Rombo syndrome: a second case report and review
is main subject of	wds:Q40908995-BAD14CAC-3746-420A-887B-27273CF21AD5 wds:Q34249414-118E1384-A74F-4D39-8121-4B7B553AD5B2 wds:Q33952661-A9099FEA-4B42-49D4-AD5A-0F2100A2DFA1

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