Alpha-mannosidosis is an inherited lysosomal storage disorder characterized by immune deficiency, facial and skeletal abnormalities, hearing impairment, and intellectual deficit. [ Orphanet:61 ]
Synonyms: Alpha-D-mannosidosis lysosomal alpha-D-mannosidase deficiency mannosidosis, alpha-, types I and II alpha-mannosidosis deficiency of alpha-mannosidase alpha-mannosidase deficiency
Term information
- MESH:D008363 (Orphanet:61/e)
- MEDGEN:7467 (MONDO:equivalentTo)
- UMLS:C0024748 (MONDO:equivalentTo)
- SCTID:65524005 (MONDO:equivalentTo)
- NORD:755 (MONDO:NORD)
- OMIM:248500 (Orphanet:61/e)
- GARD:6968 (MONDO:GARD)
- ICD9:271.8 (MONDO:relatedTo)
- DOID:3413 (MONDO:equivalentTo)
- Orphanet:61 (OMIM:248500)
- NCIT:C84548 (MONDO:equivalentTo)
- NANDO:1200126 (https://orcid.org/0000-0003-0011-764X)
gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare, clingen
http://purl.obolibrary.org/obo/DOID_3413
http://identifiers.org/mesh/D008363
http://purl.obolibrary.org/obo/NCIT_C84548
http://linkedlifedata.com/resource/umls/id/C0024748
http://www.orpha.net/ORDO/Orphanet_61
http://identifiers.org/medgen/7467
https://omim.org/entry/248500
http://identifiers.org/snomedct/65524005
Alpha-mannosidase B deficiency
MANSA
mannosidosis, ALPHA B, lysosomal
mannosidosis, alpha B lysosomal
lysosomal Alpha-D-mannosidase deficiency
Alpha mannosidase B deficiency
https://github.com/monarch-initiative/mondo/issues/4521
https://github.com/monarch-initiative/mondo/issues/4948