Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024
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Preferred Name

Laurence-Moon syndrome
Synonyms

LMS
Definitions

A very rare genetic multisystemic disorder characterized by progressive neurological, ophthalmologic and endocrine manifestations leading to severe handicap.
ID

http://www.orpha.net/ORDO/Orphanet_2377
alternative_term

LMS
definition

A very rare genetic multisystemic disorder characterized by progressive neurological, ophthalmologic and endocrine manifestations leading to severe handicap.
definition_citation

Orphanet
expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=2377
has_age_of_onset

Neonatal
has_inheritance

Autosomal recessive
hasDbXref

OMIM:245800

ICD-10:Q87.8

MedDRA:10056710

UMLS:C0023138

MeSH:D007849

ICD-11:LD90.Y
label

Laurence-Moon syndrome
notation

ORPHA:2377
part_of

http://www.orpha.net/ORDO/Orphanet_98661

http://www.orpha.net/ORDO/Orphanet_611327

http://www.orpha.net/ORDO/Orphanet_102283

http://www.orpha.net/ORDO/Orphanet_181387

http://www.orpha.net/ORDO/Orphanet_156183
prefixIRI

ORDO:Orphanet_2377
prefLabel

Laurence-Moon syndrome
present_in

Worldwide AND has_point_prevalence_range : Unknown
treeView

http://www.orpha.net/ORDO/Orphanet_98661

http://www.orpha.net/ORDO/Orphanet_611327

http://www.orpha.net/ORDO/Orphanet_102283

http://www.orpha.net/ORDO/Orphanet_181387

http://www.orpha.net/ORDO/Orphanet_156183
subClassOf

http://www.orpha.net/ORDO/Orphanet_377789

http://www.orpha.net/ORDO/Orphanet_557493
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Delete Mapping To Ontology Source
http://www.orpha.net/ORDO/Orphanet_2377 CCONT SAME_URI
http://www.orpha.net/ORDO/Orphanet_2377 EFO SAME_URI
http://www.orpha.net/ORDO/Orphanet_2377 EFO SAME_URI
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.077.509 RH-MESH LOOM
http://www.limics.org/hrdo/rdfns#pat_id_531 HRDO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.140.617.500 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D007849 RH-MESH LOOM
http://purl.bioontology.org/ontology/MESH/D007849 MESH LOOM
http://purl.obolibrary.org/obo/DOID_1930 DOID LOOM
http://purl.obolibrary.org/obo/DOID_1930 BAO LOOM
http://purl.obolibrary.org/obo/DOID_1930 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_1930 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_1930 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_1930 FNS-H LOOM
http://www.phoc.org.cn/pmo/class/PMO_00038267 PMAPP-PMO LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0023138 OCHV LOOM
http://www.semanticweb.org/hamide/ontologies/2019/3/IRD_6_4_22 HAMIDEHSGH LOOM
http://purl.obolibrary.org/obo/NCIT_C34760 BERO LOOM
http://purl.obolibrary.org/obo/OMIT_0008946 OMIT LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#7250 OCHV LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34760 NCIT LOOM
http://purl.obolibrary.org/obo/MONDO_0009514 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0009514 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0009514 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0009514 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0009514 DOVES LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_1930 NATPRO LOOM
http://purl.bioontology.org/ontology/RCD/X00e1 RCD LOOM
rgo:19288 GAMUTS LOOM
http://purl.bioontology.org/ontology/ICD10CM/Q87.84 ICD10CM LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/232059000 SNOMEDCT LOOM
http://purl.bioontology.org/ontology/MEDDRA/10056710 MEDDRA LOOM
http://id.nlm.nih.gov/mesh/D007849 MDM LOOM
http://purl.jp/bio/4/id/200906051501978183 IOBC LOOM
http://purl.bioontology.org/ontology/OMIM/245800 OMIM LOOM
http://www.gamuts.net/entity#Laurence_Moon_syndrome GAMUTS REST