multiple congenital anomalies-hypotonia-seizures syndrome
lipid metabolism disorder that is characterized by phosphatidylinositol glycan anchor biosynthesis class A (PIGA) deficiency
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multiple congenital anomalies-hypotonia-seizures syndrome
Summary
multiple congenital anomalies-hypotonia-seizures syndrome is a class of disease[1].
Key Facts
- multiple congenital anomalies-hypotonia-seizures syndrome's instance of is recorded as class of disease[2].
- multiple congenital anomalies-hypotonia-seizures syndrome's subclass of is recorded as lipid metabolism disorder[3].
- multiple congenital anomalies-hypotonia-seizures syndrome's KEGG ID is recorded as H01486[4].
- multiple congenital anomalies-hypotonia-seizures syndrome's Disease Ontology ID is recorded as DOID:0080503[5].
- multiple congenital anomalies-hypotonia-seizures syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080503[6].
- multiple congenital anomalies-hypotonia-seizures syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080503[7].
- multiple congenital anomalies-hypotonia-seizures syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[8].