Preferred Name

Lissencephaly
Synonyms

Agyria

Lissencephaly syndrome

Lissencephaly pachygyria

Lissencephaly (disorder)
ID

204036008
Full Id

http://purl.bioontology.org/ontology/SNOMEDCT/204036008
CONCEPTSTATUS

0
CTV3ID

P223.
has_associated_morphology

Congenital anomaly
has_clinical_course

Courses
has_finding_site

Brain structure
has_severity

Severities
inverse_may_be_a

Miller-Dieker syndrome
isa

Congenital anomaly of brain

Disorder of neuronal migration and differentiation
ISPRIMITIVE

1
occurs_in

Congenital
Semantic_Type

Disease or Syndrome

Congenital Abnormality
SNOMEDID

D4-9000C
SYNONYM FN

Lissencephaly (disorder)
SYNONYM SY

Agyria

Lissencephaly syndrome

Lissencephaly pachygyria
TUI

T047

T019
UMLS_CUI

C0265219

C0266463

C1879312
Create New Mapping

Mapping To Ontology Source Comment Relationship Added By Added On Notes
http://purl.bioontology.org/ontology/NDFRT/N0000181090 National Drug File NLM UMLS (CUI) CUI: C0266463 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MDR/10048911 MedDRA NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU008636 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0266463 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MSH/D054221 Medical Subject Headings (MeSH) NLM UMLS (CUI) CUI: C0265219 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q93.88 ICD10CM NLM UMLS (CUI) CUI: C0265219 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MSH/D054082 Medical Subject Headings (MeSH) NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/NDFRT/N0000181090 National Drug File NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.org/obo/owl/HP#HP_0001339 Bone Dysplasia Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MDR/10048915 MedDRA NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q04.3 ICD10CM NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MSH/D054082 Medical Subject Headings (MeSH) NLM UMLS (CUI) CUI: C0266463 skos:closeMatch loom 04/02/13 View Notes
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:1771 Fanconi Anemia (FA) Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://bioonto.de/mesh.owl#C10.500.507.249 OWL Version of MeSH NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.obolibrary.org/obo/DOID_0050453 Neuroscience Information Framework Standard ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MDR/10048911 MedDRA NLM UMLS (CUI) CUI: C0266463 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MDR/10068361 MedDRA NLM UMLS (CUI) CUI: C0265219 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/P223. Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0266463 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MDR/10048915 MedDRA NLM UMLS (CUI) CUI: C1879312 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/247200 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0265219 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU011842 Online Mendelian Inheritance in Man NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/X77r4 Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0265219 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU011842 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C1879312 skos:closeMatch loom 04/02/13 View Notes
http://purl.obolibrary.org/obo/HP_0001339 Human Phenotype Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q04.3 ICD10CM NLM UMLS (CUI) CUI: C0266463 skos:closeMatch loom 04/02/13 View Notes
http://www.owl-ontologies.com/NPOntology.owl#DOID_0050453 Natural Products Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://bioonto.de/mesh.owl#D054082 OWL Version of MeSH NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://www.orphanet.org/rdfns#pat_id_10627 Experimental Factor Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:1737 Fanconi Anemia (FA) Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://www.orphanet.org/rdfns#pat_id_10627 Orphanet Ontology of Rare Diseases NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://bioontology.org/projects/ontologies/radlex/radlexOwlDlComponent#RID3766 RadLex NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU008636 Online Mendelian Inheritance in Man NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/P223. Read Codes, Clinical Terms Version 3 (CTV3) NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.obolibrary.org/obo/DOID_0050453 Human disease ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.obolibrary.org/obo/DOID_0050453 NIF Dysfunction NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://bioonto.de/mesh.owl#C16.131.666.507.186 OWL Version of MeSH NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes

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