hypomyelinating leukodystrophy 6

Summary

hypomyelinating leukodystrophy 6 is a rare disease^[1].

Key Facts

• hypomyelinating leukodystrophy 6's instance of is recorded as rare disease^[2].
• hypomyelinating leukodystrophy 6's instance of is recorded as class of disease^[3].
• hypomyelinating leukodystrophy 6's subclass of is recorded as hypomyelinating leukodystrophy^[4].
• hypomyelinating leukodystrophy 6's subclass of is recorded as autosomal dominant disease^[5].
• hypomyelinating leukodystrophy 6's OMIM ID is recorded as 612438^[6].
• hypomyelinating leukodystrophy 6's Disease Ontology ID is recorded as DOID:0060798^[7].
• hypomyelinating leukodystrophy 6's Orphanet ID is recorded as 139441^[8].
• hypomyelinating leukodystrophy 6's NCI Thesaurus ID is recorded as C183310^[9].
• hypomyelinating leukodystrophy 6's genetic association is recorded as TUBB4A^[10].
• hypomyelinating leukodystrophy 6's genetic association is recorded as UFM1^[11].
• hypomyelinating leukodystrophy 6's exact match is recorded as http://identifiers.org/doid/DOID:0060798^[12].
• hypomyelinating leukodystrophy 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060798^[13].
• hypomyelinating leukodystrophy 6's UMLS CUI is recorded as C2676244^[14].
• hypomyelinating leukodystrophy 6's ICD-10-CM is recorded as E75.2^[15].
• hypomyelinating leukodystrophy 6's GARD rare disease ID is recorded as 10917^[16].
• hypomyelinating leukodystrophy 6's on focus list of Wikimedia project is recorded as WikiProject Medicine^[17].
• hypomyelinating leukodystrophy 6's Mondo ID is recorded as MONDO_0012905^[18].
• hypomyelinating leukodystrophy 6's UniProt disease ID is recorded as DI-03778^[19].