ZFIN Human Disease: mucopolysaccharidosis II

OBO ID: DOID:12799

Term Name:	mucopolysaccharidosis II		Search Ontology:
Synonyms:	deficiency of iduronate-2-sulphatase Hunter syndrome Hunter's syndrome MPS II - Hunter syndrome Mucopolysaccharidosis, MPS-II
Definition:	A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme iduronate sulfatase. http://en.wikipedia.org/wiki/Hunter_syndrome
References:	GARD:6675 ICD10CM:E76.1 MESH:D016532 NCI:C61260 OMIM:309900 SNOMEDCT_US_2023_03_01:190936000 UMLS_CUI:C0026705
Ontology:	Human Disease ( DOID:12799 )

Relationships

is a type of:	mucopolysaccharidosis mucopolysaccharidosis Show first 5 Terms

OTHER mucopolysaccharidosis II PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
IDS	ids	Mucopolysaccharidosis II	309900

ZEBRAFISH MODELS

Fish	Conditions	Citations
ids^ia200/ia200	standard conditions	Bellesso et al., 2018
ia4Tg + MO1-ids	standard conditions	Costa et al., 2017
ia5Tg + MO1-ids	standard conditions	Costa et al., 2017
ia11Tg + MO1-ids	standard conditions	Costa et al., 2017
ia18Tg + MO1-ids	standard conditions	Costa et al., 2017
ia10Tg; ia11Tg + MO1-ids	standard conditions	Costa et al., 2017
el108Tg + MO1-ids	standard conditions	Costa et al., 2017
el108Tg; ia10Tg + MO1-ids	standard conditions	Costa et al., 2017

PHENOTYPE No data available

CITATIONS (3)