ZFIN Human Disease: chromosome 18p deletion syndrome

OBO ID: DOID:0060406

Term Name:	chromosome 18p deletion syndrome		Search Ontology:
Synonyms:	18p- syndrome De Grouchy syndrome monosomy 18p
Definition:	A chromosomal deletion syndrome that has_material_basis_in partial or complete deletion of the short arm of chromosome 18. https://pubmed.ncbi.nlm.nih.gov/16691587
References:	GARD:8631 MESH:C538309 NCI:C84521 OMIM:146390 ORDO:1598 SNOMEDCT_US_2023_03_01:205632001 UMLS_CUI:C0432442
Ontology:	Human Disease ( DOID:0060406 )

Relationships

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

OTHER chromosome 18p deletion syndrome PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None