ZFIN Human Disease: posterior amorphous corneal dystrophy

OBO ID: DOID:0060452

Term Name:	posterior amorphous corneal dystrophy		Search Ontology:
Synonyms:	chromosome 12q21.33 deletion syndrome PACD
Definition:	A stromal dystrophy that is characterized by irregular sheetlike areas of opacification with involvement of the Descemet membrane and, in some instances, alterations of the normal endothelial mosaic and that has_material_basis_in a chromosome 12q21.33 contiguous gene deletion syndrome. https://pubmed.ncbi.nlm.nih.gov/27096414/
References:	ICD10CM:H18.5 MESH:C567546 OMIM:612868 ORDO:98971
Ontology:	Human Disease ( DOID:0060452 )

Relationships

is a type of:	autosomal dominant disease chromosomal deletion syndrome stromal dystrophy autosomal dominant disease chromosomal deletion syndrome stromal dystrophy Show first 5 Terms

OTHER posterior amorphous corneal dystrophy PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None