hypomyelinating leukodystrophy 11

Summary

hypomyelinating leukodystrophy 11 is a rare disease^[1].

Key Facts

• hypomyelinating leukodystrophy 11's instance of is recorded as rare disease^[2].
• hypomyelinating leukodystrophy 11's instance of is recorded as class of disease^[3].
• hypomyelinating leukodystrophy 11's subclass of is recorded as hypomyelinating leukodystrophy^[4].
• hypomyelinating leukodystrophy 11's subclass of is recorded as autosomal recessive disease^[5].
• hypomyelinating leukodystrophy 11's OMIM ID is recorded as 616494^[6].
• hypomyelinating leukodystrophy 11's Disease Ontology ID is recorded as DOID:0060792^[7].
• hypomyelinating leukodystrophy 11's health specialty is recorded as neurology^[8].
• hypomyelinating leukodystrophy 11's genetic association is recorded as POLR1C^[9].
• hypomyelinating leukodystrophy 11's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060792^[10].
• hypomyelinating leukodystrophy 11's exact match is recorded as http://identifiers.org/doid/DOID:0060792^[11].
• hypomyelinating leukodystrophy 11's UMLS CUI is recorded as C4225305^[12].
• hypomyelinating leukodystrophy 11's ICD-10-CM is recorded as G11.1^[13].
• hypomyelinating leukodystrophy 11's on focus list of Wikimedia project is recorded as WikiProject Medicine^[14].
• hypomyelinating leukodystrophy 11's Mondo ID is recorded as MONDO_0014666^[15].
• hypomyelinating leukodystrophy 11's UniProt disease ID is recorded as DI-04497^[16].