About: Hereditary Optic Atrophy

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About: Hereditary Optic Atrophy Goto Sponge NotDistinct Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

Attributes	Values
rdf:type	Class
rdfs:label	Hereditary Optic Atrophy
rdfs:subClassOf	Optic Atrophy nodeID://b679853
Semantic_Type	Congenital Abnormality Disease or Syndrome
Preferred_Name	Hereditary Optic Atrophy
UMLS_CUI	C0029125
ALT_DEFINITION	Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER).MSH2003_2003_05_12
Legacy_Concept_Name	Hereditary_Optic_Atrophy
FULL_SYN	Hereditary Optic AtrophyPTNCI
code	C34864
http://linked.open...y/mesh/hasConcept	http://linked.opendata.cz/resource/mesh/concept/M0023768
is rdfs:subClassOf of	Optic Atrophy, Hereditary, Leber Optic Atrophy, Autosomal Dominant
is sameAs of	Optic Atrophies, Hereditary

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