ZFIN Human Disease: chromosome 13q14 deletion syndrome

OBO ID: DOID:0060391

Term Name:	chromosome 13q14 deletion syndrome		Search Ontology:
Synonyms:	deletion 13q14
Definition:	A chromosomal deletion syndrome that is characterized by low birth weight, dysmorphic facies, limb defects, genital malformations and psychomotor developmental delay, has_material_basis_in deletion of the long arm of chromosome 13. https://rarediseases.org/rare-diseases/chromosome-13-partial-monosomy-13q/
References:	ICD10CM:Q93.5 OMIM:613884 ORDO:1587
Ontology:	Human Disease ( DOID:0060391 )

Relationships

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

OTHER chromosome 13q14 deletion syndrome PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None