Disease #04075 (MSCCA (microcephaly, progressive, seizures, and cerebral and cerebellar atrophy (MSCCA)), OMIM:615760)

Official abbreviation MSCCA
Name microcephaly, progressive, seizures, and cerebral and cerebellar atrophy (MSCCA)
OMIM ID 615760
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene QARS
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00092269 - PubMed: Tarailo-Graovac 2016, Journal: Tarailo-Graovac 2016 - - - United States - - - - - MSCCA profound IDD with developmental arrest, progressive microcephaly with diffuse supra-tentorial cerebral atrophy & severely deficient myelination, intractable seizures; serine deficiency QARS QARS 2 1 Johan den Dunnen
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