Zellweger spectrum disorder
group of rare autosomal recessive genetic disorders
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Zellweger spectrum disorder
Summary
Zellweger spectrum disorder is a class of disease[1].
Key Facts
- Zellweger spectrum disorder's instance of is recorded as class of disease[2].
- Hans Zellweger is named after Zellweger spectrum disorder[3].
- Zellweger spectrum disorder's subclass of is recorded as peroxisomal disease[4].
- Zellweger spectrum disorder's subclass of is recorded as nervous system heredodegenerative disease[5].
- Zellweger spectrum disorder's subclass of is recorded as neurometabolic disease[6].
- Zellweger spectrum disorder's subclass of is recorded as rare hereditary metabolic disease with peripheral neuropathy[7].
- Zellweger spectrum disorder's subclass of is recorded as rare metabolic liver disease[8].
- Zellweger spectrum disorder's MeSH descriptor ID is recorded as C536664[9].
- Zellweger spectrum disorder's OMIM ID is recorded as 601539[10].
- Zellweger spectrum disorder's KEGG ID is recorded as H00205[11].
- Zellweger spectrum disorder's Orphanet ID is recorded as 79189[12].
- Zellweger spectrum disorder's NCI Thesaurus ID is recorded as C146639[13].
- Zellweger spectrum disorder's genetic association is recorded as PEX1[14].
- Zellweger spectrum disorder's genetic association is recorded as PEX10[15].
- Zellweger spectrum disorder's genetic association is recorded as PEX11B[16].
- Zellweger spectrum disorder's genetic association is recorded as PEX12[17].
- Zellweger spectrum disorder's genetic association is recorded as PEX13[18].
- Zellweger spectrum disorder's genetic association is recorded as PEX14[19].
- Zellweger spectrum disorder's genetic association is recorded as PEX16[20].
- Zellweger spectrum disorder's genetic association is recorded as PEX19[21].
- Zellweger spectrum disorder's genetic association is recorded as PEX2[22].
- Zellweger spectrum disorder's genetic association is recorded as PEX26[23].
- Zellweger spectrum disorder's genetic association is recorded as PEX3[24].
- Zellweger spectrum disorder's genetic association is recorded as PEX5[25].
- Zellweger spectrum disorder's genetic association is recorded as PEX6[26].