ZFIN Human Disease: frontonasal dysplasia 3

OBO ID: DOID:0081047

Term Name:	frontonasal dysplasia 3		Search Ontology:
Synonyms:
Definition:	A frontonasal dysplasia that has_material_basis_in homozygous mutation in the ALX1 gene on chromosome 12q21. (2)
References:	OMIM:613456
Ontology:	Human Disease ( DOID:0081047 )

Relationships

is a type of:	autosomal recessive disease frontonasal dysplasia autosomal recessive disease frontonasal dysplasia Show first 5 Terms

OTHER frontonasal dysplasia 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ALX1	alx1	Frontonasal dysplasia 3	613456

ZEBRAFISH MODELS

Fish	Conditions	Citations
alx1^{uw2016/uw2016} (NHGRI-1)	standard conditions	Pini et al., 2020
WT + MO1-alx1	standard conditions	Dee et al., 2013

PHENOTYPE No data available

CITATIONS (3)