Kidney Tissue Atlas Ontology

Last uploaded: March 16, 2024
Preferred Name

genetic multiple congenital anomalies/dysmorphic syndrome
Synonyms

hereditary multiple congenital anomalies/dysmorphic syndrome

Definitions

An instance of multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome.

ID

http://purl.obolibrary.org/obo/MONDO_0043005

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml

database_cross_reference

Orphanet:183533

exactMatch

http://www.orpha.net/ORDO/Orphanet_183533

has exact synonym

hereditary multiple congenital anomalies/dysmorphic syndrome

has modifier

http://purl.obolibrary.org/obo/MONDO_0021136

id

MONDO:0043005

imported from

http://purl.obolibrary.org/obo/mondo.owl

in_subset

http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders

label

genetic multiple congenital anomalies/dysmorphic syndrome

notation

MONDO:0043005

prefLabel

genetic multiple congenital anomalies/dysmorphic syndrome

textual definition

An instance of multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome.

subClassOf

http://purl.obolibrary.org/obo/MONDO_0019042

http://purl.obolibrary.org/obo/MONDO_0003847

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