mucolipidosis type III gamma
human disease
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mucolipidosis type III gamma
Summary
mucolipidosis type III gamma is a class of disease[1].
Key Facts
- mucolipidosis type III gamma's instance of is recorded as class of disease[2].
- mucolipidosis type III gamma's subclass of is recorded as pseudo-Hurler polydystrophy[3].
- mucolipidosis type III gamma's subclass of is recorded as mucolipidosis[4].
- mucolipidosis type III gamma's subclass of is recorded as autosomal recessive disease[5].
- mucolipidosis type III gamma's MeSH descriptor ID is recorded as C565367[6].
- mucolipidosis type III gamma's OMIM ID is recorded as 252605[7].
- mucolipidosis type III gamma's Disease Ontology ID is recorded as DOID:0080678[8].
- mucolipidosis type III gamma's Orphanet ID is recorded as 423470[9].
- mucolipidosis type III gamma's NCI Thesaurus ID is recorded as C129978[10].
- mucolipidosis type III gamma's genetic association is recorded as GNPTG[11].
- mucolipidosis type III gamma's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_423470[12].
- mucolipidosis type III gamma's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_577[13].
- mucolipidosis type III gamma's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080678[14].
- mucolipidosis type III gamma's exact match is recorded as http://identifiers.org/doid/DOID:0080678[15].
- mucolipidosis type III gamma's UMLS CUI is recorded as C1854896[16].
- mucolipidosis type III gamma's ICD-10-CM is recorded as E77.0[17].
- mucolipidosis type III gamma's Mondo ID is recorded as MONDO_0009652[18].