Digital medicine Outcomes Value Set (DOVeS) Ontology

Last uploaded: December 13, 2023
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Preferred Name

Crouzon syndrome
Synonyms

craniofacial dysostosis, type 1

Crouzon's disease

craniofacial dysostosis type 1

Crouzon disease

Cfd1

craniofacial dysostosis

Crouzon syndrome

Crouzon craniofacial dysostosis
Definitions

Crouzon disease is characterized by craniosynostosis and facial hypoplasia.
ID

http://purl.obolibrary.org/obo/MONDO_0007405
altLabel

craniofacial dysostosis, type 1

Crouzon's disease

craniofacial dysostosis type 1

Crouzon disease

Cfd1

craniofacial dysostosis

Crouzon syndrome

Crouzon craniofacial dysostosis
definition

Crouzon disease is characterized by craniosynostosis and facial hypoplasia.
has_exact_synonym

craniofacial dysostosis

Crouzon syndrome

Crouzon craniofacial dysostosis
has_related_synonym

craniofacial dysostosis, type 1

Crouzon's disease

craniofacial dysostosis type 1

Crouzon disease

Cfd1
IAO_0000233

https://github.com/monarch-initiative/mondo/issues/4948
label

Crouzon syndrome
prefixIRI

MONDO:0007405
prefLabel

Crouzon syndrome
seeAlso

https://rarediseases.info.nih.gov/diseases/6206/crouzon-syndrome
textual definition

Crouzon disease is characterized by craniosynostosis and facial hypoplasia.
subClassOf

http://purl.obolibrary.org/obo/MONDO_0015338

http://purl.obolibrary.org/obo/MONDO_0015368
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http://purl.obolibrary.org/obo/MONDO_0007405 MONDO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0007405 EFO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0007405 CCONT SAME_URI
http://purl.obolibrary.org/obo/MONDO_0007405 HSPO SAME_URI
http://purl.obolibrary.org/obo/DOID_2339 DDSS LOOM
http://purl.obolibrary.org/obo/MONDO_0007405 MONDO LOOM
http://www.orpha.net/ORDO/Orphanet_207 ORDO LOOM
http://purl.obolibrary.org/obo/MONDO_0007405 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0007405 HSPO LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_2339 NATPRO LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0010273 OCHV LOOM
http://www.owl-ontologies.com/Ontology1358660052.owl#Crouzon_Syndrome PEDTERM LOOM
http://identifiers.org/omim/123500 REXO LOOM
http://identifiers.org/omim/123500 GEXO LOOM
http://identifiers.org/omim/123500 RETO LOOM
http://www.orpha.net/ORDO/Orphanet_207 ORDO LOOM
http://purl.obolibrary.org/obo/DOID_2339 DTO LOOM
http://purl.obolibrary.org/obo/DOID_2339 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_2339 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_2339 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_2339 FNS-H LOOM
http://purl.bioontology.org/ontology/RCD/PG04. RCD LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/28861008 SNOMEDCT LOOM
http://www.owl-ontologies.com/unnamed.owl#RID17907 DERMLEX LOOM
http://purl.bioontology.org/ontology/OMIM/123500 OMIM LOOM
http://purl.bioontology.org/ontology/SNMI/D4-00C05 SNMI LOOM
http://purl.obolibrary.org/obo/OMIM_123500 CCO LOOM
http://purl.obolibrary.org/obo/HIO_0000193 HIO LOOM
http://purl.org/skeletome/bonedysplasia#Crouzon_syndrome BDO LOOM
http://purl.obolibrary.org/obo/MONDO_0007405 EFO LOOM
http://purl.obolibrary.org/obo/DOID_2339 CLO LOOM
http://purl.obolibrary.org/obo/DOID_2339 DOID LOOM
rgo:08707 GAMUTS LOOM