hypomyelinating leukodystrophy 12

Summary

hypomyelinating leukodystrophy 12 is a rare disease^[1].

Key Facts

• hypomyelinating leukodystrophy 12's instance of is recorded as rare disease^[2].
• hypomyelinating leukodystrophy 12's instance of is recorded as class of disease^[3].
• hypomyelinating leukodystrophy 12's subclass of is recorded as hypomyelinating leukodystrophy^[4].
• hypomyelinating leukodystrophy 12's subclass of is recorded as genetic syndromic intellectual disability^[5].
• hypomyelinating leukodystrophy 12's subclass of is recorded as autosomal recessive disease^[6].
• hypomyelinating leukodystrophy 12's OMIM ID is recorded as 616683^[7].
• hypomyelinating leukodystrophy 12's Disease Ontology ID is recorded as DOID:0060796^[8].
• hypomyelinating leukodystrophy 12's Orphanet ID is recorded as 466934^[9].
• hypomyelinating leukodystrophy 12's genetic association is recorded as VPS11^[10].
• hypomyelinating leukodystrophy 12's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060796^[11].
• hypomyelinating leukodystrophy 12's exact match is recorded as http://identifiers.org/doid/DOID:0060796^[12].
• hypomyelinating leukodystrophy 12's UMLS CUI is recorded as C4225247^[13].
• hypomyelinating leukodystrophy 12's on focus list of Wikimedia project is recorded as WikiProject Medicine^[14].
• hypomyelinating leukodystrophy 12's Mondo ID is recorded as MONDO_0014732^[15].
• hypomyelinating leukodystrophy 12's UniProt disease ID is recorded as DI-04619^[16].