hypomyelinating leukodystrophy 3

Summary

hypomyelinating leukodystrophy 3 is a rare disease^[1].

Key Facts

• hypomyelinating leukodystrophy 3's instance of is recorded as rare disease^[2].
• hypomyelinating leukodystrophy 3's instance of is recorded as class of disease^[3].
• hypomyelinating leukodystrophy 3's subclass of is recorded as hypomyelinating leukodystrophy^[4].
• hypomyelinating leukodystrophy 3's subclass of is recorded as autosomal recessive disease^[5].
• hypomyelinating leukodystrophy 3's OMIM ID is recorded as 260600^[6].
• hypomyelinating leukodystrophy 3's Disease Ontology ID is recorded as DOID:0060790^[7].
• hypomyelinating leukodystrophy 3's Orphanet ID is recorded as 280293^[8].
• hypomyelinating leukodystrophy 3's genetic association is recorded as AIMP1^[9].
• hypomyelinating leukodystrophy 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060790^[10].
• hypomyelinating leukodystrophy 3's exact match is recorded as http://identifiers.org/doid/DOID:0060790^[11].
• hypomyelinating leukodystrophy 3's UMLS CUI is recorded as C5396702^[12].
• hypomyelinating leukodystrophy 3's ICD-10-CM is recorded as E75.2^[13].
• hypomyelinating leukodystrophy 3's GARD rare disease ID is recorded as 4266^[14].
• hypomyelinating leukodystrophy 3's on focus list of Wikimedia project is recorded as WikiProject Medicine^[15].
• hypomyelinating leukodystrophy 3's Mondo ID is recorded as MONDO_0009843^[16].
• hypomyelinating leukodystrophy 3's UniProt disease ID is recorded as DI-03001^[17].