hypomyelinating leukodystrophy 13

Summary

hypomyelinating leukodystrophy 13 is a rare disease^[1].

Key Facts

• hypomyelinating leukodystrophy 13's instance of is recorded as rare disease^[2].
• hypomyelinating leukodystrophy 13's instance of is recorded as class of disease^[3].
• hypomyelinating leukodystrophy 13's subclass of is recorded as hypomyelinating leukodystrophy^[4].
• hypomyelinating leukodystrophy 13's subclass of is recorded as autosomal recessive disease^[5].
• hypomyelinating leukodystrophy 13's OMIM ID is recorded as 616881^[6].
• hypomyelinating leukodystrophy 13's Disease Ontology ID is recorded as DOID:0060795^[7].
• hypomyelinating leukodystrophy 13's genetic association is recorded as HIKESHI^[8].
• hypomyelinating leukodystrophy 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060795^[9].
• hypomyelinating leukodystrophy 13's exact match is recorded as http://identifiers.org/doid/DOID:0060795^[10].
• hypomyelinating leukodystrophy 13's UMLS CUI is recorded as C4225170^[11].
• hypomyelinating leukodystrophy 13's on focus list of Wikimedia project is recorded as WikiProject Medicine^[12].
• hypomyelinating leukodystrophy 13's Mondo ID is recorded as MONDO_0014813^[13].
• hypomyelinating leukodystrophy 13's UniProt disease ID is recorded as DI-04695^[14].