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Metadata
ID DOID:0110120
Name Axenfeld-Rieger syndrome type 1
Definition An Axenfeld-Rieger syndrome that has_material_basis_in heterozygous mutation in the homeobox transcription factor gene PITX2 on chromosome 4q25.
https://www.ncbi.nlm.nih.gov/pubmed/8944018
Xrefs

ICD10CM:Q13.8

OMIM:180500

Synonyms

RIEG1 [EXACT]

Rieger syndrome type 1 [EXACT]

Parent Relationships

is_a Axenfeld-Rieger syndrome

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