ZFIN Human Disease: autosomal recessive congenital nystagmus

OBO ID: DOID:0111797

OBO ID: DOID:0111797

Term Name:	autosomal recessive congenital nystagmus	Search Ontology:
Synonyms:	autosomal recessive congenital motor nystagmus
Definition:	A congenital nystagmus characterized by autosomal recessive inheritance. https://europepmc.org/article/med/305814
References:	GARD:9609 OMIM:257400
Ontology:	Human Disease ( DOID:0111797 )

Relationships

is a type of:	autosomal recessive disease congenital nystagmus autosomal recessive disease congenital nystagmus Show first 5 Terms

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ROBO1	robo1	?Nystagmus 8, congenital, autosomal recessive	257400

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None