hypomyelinating leukodystrophy 10
Human disease
Press Enter · cited answer in seconds
0 sources
hypomyelinating leukodystrophy 10
Summary
hypomyelinating leukodystrophy 10 is a rare disease[1].
Key Facts
- hypomyelinating leukodystrophy 10's instance of is recorded as rare disease[2].
- hypomyelinating leukodystrophy 10's instance of is recorded as class of disease[3].
- hypomyelinating leukodystrophy 10's subclass of is recorded as hypomyelinating leukodystrophy[4].
- hypomyelinating leukodystrophy 10's subclass of is recorded as autosomal recessive disease[5].
- hypomyelinating leukodystrophy 10's OMIM ID is recorded as 616420[6].
- hypomyelinating leukodystrophy 10's Disease Ontology ID is recorded as DOID:0060788[7].
- hypomyelinating leukodystrophy 10's genetic association is recorded as PYCR2[8].
- hypomyelinating leukodystrophy 10's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060788[9].
- hypomyelinating leukodystrophy 10's exact match is recorded as http://identifiers.org/doid/DOID:0060788[10].
- hypomyelinating leukodystrophy 10's UMLS CUI is recorded as C4225332[11].
- hypomyelinating leukodystrophy 10's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- hypomyelinating leukodystrophy 10's Mondo ID is recorded as MONDO_0014632[13].
- hypomyelinating leukodystrophy 10's UniProt disease ID is recorded as DI-04450[14].