ZFIN Human Disease: Alport syndrome

OBO ID: DOID:10983

Term Name:	Alport syndrome		Search Ontology:
Synonyms:	Hereditary Nephritis
Definition:	A syndrome disease that is characterized by glomerulonephritis, endstage kidney disease, and hearing loss. http://en.wikipedia.org/wiki/Alport_syndrome
References:	GARD:5785 MESH:D009394 ORDO:63 SNOMEDCT_US_2023_03_01:57333009 UMLS_CUI:C0027706
Ontology:	Human Disease ( DOID:10983 )

Relationships

is a type of:	monogenic disease syndrome monogenic disease syndrome Show first 5 Terms
has subtype:	autosomal dominant Alport syndrome autosomal recessive Alport syndrome X-linked Alport syndrome autosomal dominant Alport syndrome autosomal recessive Alport syndrome X-linked Alport syndrome Show first 5 Terms

OTHER Alport syndrome PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS

Fish	Conditions	Citations
WT + CRISPR1-col4a3 + CRISPR2-col4a3 + CRISPR3-col4a3 + CRISPR4-col4a3	standard conditions	Naylor et al., 2022
WT + CRISPR1-col4a4 + CRISPR2-col4a4 + CRISPR3-col4a4 + CRISPR4-col4a4	standard conditions	Naylor et al., 2022

PHENOTYPE No data available

CITATIONS (1)