Preferred Name

Porokeratosis of Mibelli
Synonyms

Porokeratosis

Mibelli's disease

Porokeratosis of Mibelli (disorder)

Porokeratosis, NOS
ID

80432009
Full Id

http://purl.bioontology.org/ontology/SNOMEDCT/80432009
CONCEPTSTATUS

0
CTV3ID

X507F
has_associated_morphology

Hyperkeratosis

Congenital anomaly

Squamous cell neoplasm

Plaque

Eruption
has_definitional_manifestation

Abnormal keratinization
has_finding_site

Skin structure
isa

Porokeratosis

Congenital anomaly of skin

Eruption

Degenerative disorder
ISPRIMITIVE

1
occurs_in

Congenital
same_as

Porokeratosis

Mibelli's disease

Porokeratosis of Mibelli
Semantic_Type

Congenital Abnormality

Disease or Syndrome
SNOMEDID

D4-40160
SYNONYM FN

Porokeratosis of Mibelli (disorder)
SYNONYM IS

Porokeratosis, NOS
SYNONYM SY

Porokeratosis

Mibelli's disease
TUI

T019

T047
UMLS_CUI

C0162839

C0949506
Create New Mapping

Mapping To Ontology Source Comment Relationship Added By Added On Notes
http://bioonto.de/mesh.owl#C17.800.428.750 OWL Version of MeSH NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://www.orphanet.org/rdfns#pat_id_8653 Orphanet Ontology of Rare Diseases NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://www.orphanet.org/rdfns#pat_id_8653 Experimental Factor Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/X507F Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0949506 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MDR/10036175 MedDRA NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MDR/10036175 MedDRA NLM UMLS (CUI) CUI: C0162839 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/NDFRT/N0000003590 National Drug File NLM UMLS (CUI) CUI: C0162839 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MSH/D017499 Medical Subject Headings (MeSH) NLM UMLS (CUI) CUI: C0162839 skos:closeMatch loom 04/02/13 View Notes
http://bioonto.de/mesh.owl#D017499 OWL Version of MeSH NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.org/obo/owl/HP#HP_0200044 Bone Dysplasia Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/175800 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0949506 skos:closeMatch loom 04/02/13 View Notes
http://purl.obolibrary.org/obo/HP_0200044 Human Phenotype Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/PH332 Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0949506 skos:closeMatch loom 04/02/13 View Notes
http://www.owl-ontologies.com/NPOntology.owl#DOID_3805 Natural Products Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/175800 Online Mendelian Inheritance in Man NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.obolibrary.org/obo/DOID_3805 Human disease ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://bioonto.de/mesh.owl#C17.800.827.730 OWL Version of MeSH NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/X507F Read Codes, Clinical Terms Version 3 (CTV3) NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MSH/D017499 Medical Subject Headings (MeSH) NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/X507E Read Codes, Clinical Terms Version 3 (CTV3) NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.obolibrary.org/obo/DOID_3805 Neuroscience Information Framework Standard ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Porokeratosis NCI Thesaurus NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://bioonto.de/mesh.owl#C16.320.850.730 OWL Version of MeSH NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU022465 Online Mendelian Inheritance in Man NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/X507E Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0162839 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/PH332 Read Codes, Clinical Terms Version 3 (CTV3) NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://www.orphanet.org/rdfns#pat_id_11384 Orphanet Ontology of Rare Diseases NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU022465 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0162839 skos:closeMatch loom 04/02/13 View Notes
http://purl.obolibrary.org/obo/DOID_3805 NIF Dysfunction NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes

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