Preferred Name

Ablepharon
Synonyms

Complete ablepharon

Congenital absence of eyelid

Ablepharon - absent eyelids

Agenesis of eyelid

Ablepharia

Open eye

Ablepharon (disorder)
ID

13401001
Full Id

http://purl.bioontology.org/ontology/SNOMEDCT/13401001
CONCEPTSTATUS

0
CTV3ID

P3610
has_associated_morphology

Congenital absence
has_clinical_course

Courses
has_finding_site

Eyelid structure
has_severity

Severities
isa

Congenital anomaly of eyelid

Congenital malformation
ISPRIMITIVE

0
occurs_in

Congenital
same_as

Agenesis of eyelid
Semantic_Type

Congenital Abnormality
SNOMEDID

D4-A0820
SYNONYM FN

Ablepharon (disorder)
SYNONYM SY

Complete ablepharon

Congenital absence of eyelid

Ablepharon - absent eyelids

Agenesis of eyelid

Ablepharia

Open eye
TUI

T019
UMLS_CUI

C0266574
Create New Mapping

Mapping To Ontology Source Comment Relationship Added By Added On Notes
http://purl.bioontology.org/ontology/RCD/P3610 Read Codes, Clinical Terms Version 3 (CTV3) NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/RCD/P3621 Read Codes, Clinical Terms Version 3 (CTV3) NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.obolibrary.org/obo/HP_0011224 Human Phenotype Ontology NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU027595 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0266574 skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/RCD/P3610 Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0266574 skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/RCD/P3621 Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0266574 skos:closeMatch loom 05/21/13 View Notes
http://purl.org/obo/owl/HP#HP_0011224 Bone Dysplasia Ontology NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU010682 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0266574 skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q10.3 ICD10CM NLM UMLS (CUI) CUI: C0266574 skos:closeMatch loom 05/21/13 View Notes
http://uwhealth.org/himc/icd/icd09/#743.62 ICD09 NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU027595 Online Mendelian Inheritance in Man NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q10.3 ICD10CM NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes

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