ZFIN Human Disease: Tukel syndrome

OBO ID: DOID:0081021

Term Name:	Tukel syndrome		Search Ontology:
Synonyms:	congenital fibrosis of the extraocular muscles 4
Definition:	A congenital fibrosis of the extraocular muscles that is characterized by nonprogressive restrictive ophthalmoplegia with blepharoptosis of the right eye and postaxial oligodactyly/oligosyndactyly of the hands, with the right more severely affected than the left. https://pubmed.ncbi.nlm.nih.gov/15863670/
References:	GARD:9814 MESH:C536925 OMIM:609428
Ontology:	Human Disease ( DOID:0081021 )

Relationships

is a type of:	autosomal recessive disease congenital fibrosis of the extraocular muscles autosomal recessive disease congenital fibrosis of the extraocular muscles Show first 5 Terms

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Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None