Mondo Disease Ontology

Last uploaded: May 9, 2024

Preferred Name	epidermolysis bullosa dystrophica Neurotrophica
Synonyms	epidermolysis bullosa progressiva, recessive epidermolysis bullosa with congenital deafness epidermolysis bullosa dystrophica Neurotrophica
ID	http://purl.obolibrary.org/obo/MONDO_0009178
database_cross_reference	SCTID:254176007 ICD9:757.39 OMIM:226500 MESH:C562637
exactMatch	http://identifiers.org/snomedct/254176007 https://omim.org/entry/226500 http://identifiers.org/mesh/C562637
has_exact_synonym	epidermolysis bullosa dystrophica Neurotrophica
has_related_synonym	epidermolysis bullosa progressiva, recessive epidermolysis bullosa with congenital deafness
id	MONDO:0009178
in_subset	http://purl.obolibrary.org/obo/mondo#rare http://purl.obolibrary.org/obo/mondo#nord_rare
label	epidermolysis bullosa dystrophica Neurotrophica
notation	MONDO:0009178
prefLabel	epidermolysis bullosa dystrophica Neurotrophica
treeView	http://purl.obolibrary.org/obo/MONDO_0006543
subClassOf	http://purl.obolibrary.org/obo/MONDO_0006543

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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/MONDO_0009178	DOVES	SAME_URI
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C562637	RH-MESH	LOOM
http://purl.obolibrary.org/obo/MONDO_0009178	DOVES	LOOM
http://purl.bioontology.org/ontology/MESH/C562637	MESH	LOOM
http://purl.bioontology.org/ontology/OMIM/226500	OMIM	LOOM