MCID: ZLL010
MIFTS: 13
|
Zellweger-Like Syndrome Without Peroxisomal Anomalies
Categories:
Metabolic diseases, Neuronal diseases, Rare diseases
|
|
MalaCards integrated aliases for Zellweger-Like Syndrome Without Peroxisomal Anomalies:
Name: Zellweger-Like Syndrome Without Peroxisomal Anomalies
58
Characteristics:Orphanet epidemiological data:58
zellweger-like syndrome without peroxisomal anomalies
Inheritance: Autosomal recessive,Mitochondrial inheritance; Prevalence: <1/1000000 (Worldwide); Age of onset: Childhood; Classifications:
ICD10:
33
Orphanet: 58
![]() ![]() |
MalaCards based summary :
Zellweger-Like Syndrome Without Peroxisomal Anomalies, is also known as ahn-lerman-sagie syndrome. Affiliated tissues include skin, and related phenotypes are global developmental delay and muscular hypotonia
|
|
Human phenotypes related to Zellweger-Like Syndrome Without Peroxisomal Anomalies:58 31 (show all 22)
|
|
MalaCards organs/tissues related to Zellweger-Like Syndrome Without Peroxisomal Anomalies:40
Skin
|
|
Search
GEO
for disease gene expression data for Zellweger-Like Syndrome Without Peroxisomal Anomalies.
|
|
|