Medical Subject Headings

Last uploaded: November 5, 2019

Preferred Name	Behr syndrome
Synonyms	Optic Atrophy, Infantile Hereditary, With Neurologic Abnormalities
ID	http://purl.bioontology.org/ontology/MESH/C537669
altLabel	Optic Atrophy, Infantile Hereditary, With Neurologic Abnormalities Optic atrophy, infantile hereditary, Behr complicated form of
cui	C0221061
Has mapping qualifier	http://purl.bioontology.org/ontology/MESH/Q000151
HM	D008607 D013035 D001259 D009896/Q000151 D034381
Inverse of RB	0
Mapped to	http://purl.bioontology.org/ontology/MESH/D001259 http://purl.bioontology.org/ontology/MESH/D034381 http://purl.bioontology.org/ontology/MESH/D008607 http://purl.bioontology.org/ontology/MESH/D009896 http://purl.bioontology.org/ontology/MESH/D013035
MDA	20100825
MeSH Frequency	14
MMR	20131106
notation	C537669
prefLabel	Behr syndrome
SC	3
Scope Statement	Optic atrophy in early childhood, associated with ataxia, spasticity, mental retardation, and posterior column sensory loss
TERMUI	T743350 T800738 T743351
TH	ORD (2010) OMIM (2013)
tui	T047

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/OMIM/210000	Online Mendelian Inheritance in Man	CUI
http://purl.bioontology.org/ontology/OMIM/210000	Online Mendelian Inheritance in Man	LOOM
http://purl.obolibrary.org/obo/DOID_0111580	Human Disease Ontology 123	LOOM
http://purl.bioontology.org/ontology/OMIM/605290	Online Mendelian Inheritance in Man	CUI