ZFIN Human Disease: branchiootorenal syndrome

OBO ID: DOID:14702

Term Name:	branchiootorenal syndrome		Search Ontology:
Synonyms:	Branchio-Oto-renal syndrome Branchio-otorenal dysplasia branchiootorenal dysplasia Melnick-Fraser syndrome
Definition:	A syndrome characterized by branchial arch anomalies (branchial fistulas, clefts, or cysts), hearing impairment, structural defects of the outer, middle, and inner ear, and renal abnormalities. https://www.ncbi.nlm.nih.gov/pubmed/263442
References:	GARD:10147 MEDDRA:10071135 MESH:D019280 NCI:C98983 SNOMEDCT_US_2023_03_01:290006 UMLS_CUI:C0265234
Ontology:	Human Disease ( DOID:14702 )

Relationships

is a type of:	autosomal dominant disease syndrome autosomal dominant disease syndrome Show first 5 Terms
has subtype:	branchiootorenal syndrome 1 branchiootorenal syndrome 2 branchiootorenal syndrome 1 branchiootorenal syndrome 2 Show first 5 Terms

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Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None