ZFIN Human Disease: Prieto syndrome

OBO ID: DOID:0060805

Term Name:	Prieto syndrome		Search Ontology:
Synonyms:	Prieto-Badia-Mulas syndrome X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome
Definition:	A syndromic X-linked intellectual disability characterized by intellectual disability, facial dysmorphism, patella luxation, clinodactyly, subcortical cerebral atrophy, and abnormal growth of the teeth that has_material_basis_in variation in the chromosome region Xp11-q21. (2)
References:	OMIM:309610 ORDO:2958
Ontology:	Human Disease ( DOID:0060805 )

Relationships

is a type of:	syndromic X-linked intellectual disability X-linked recessive disease syndromic X-linked intellectual disability X-linked recessive disease Show first 5 Terms

OTHER Prieto syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
WNK3	wnk3	Prieto syndrome	309610

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None