ZFIN Human Disease: Currarino syndrome

OBO ID: DOID:0111546

Term Name:	Currarino syndrome		Search Ontology:
Synonyms:	Currarino triad
Definition:	A syndrome characterized by anorectal malformations, a presacral mass, and partial sacral agenesis with intact first sacral vertebra that has_material_basis_in heterozygous mutation in HLXB9 on chromosome 7q36.3. (2)
References:	GARD:1626 MESH:C536221 OMIM:176450 ORDO:1552 SNOMEDCT_US_2023_03_01:413936007 UMLS_CUI:C1531773
Ontology:	Human Disease ( DOID:0111546 )

Relationships

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

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MNX1	mnx1	Currarino syndrome	176450

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None