Disease #01937 (MPS4A (mucopolysaccharidosis, type IVA (MPS-4A)), OMIM:253000)

Official abbreviation MPS4A
Name mucopolysaccharidosis, type IVA (MPS-4A)
OMIM ID 253000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene GALNS
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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00418704 Fam7 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected carrier mother M - - - - - - - MPS4A, NDD speech delay; motor delay; intellectual disability; autism spectrum disorder; behavioral problems; facial dysmorphism; cryptorchidism, enuresis; short stature; mild features MPS4A (skeletal phenotype) caused by GALNS variants - GALNS, ZMYM3 3 1 Johan den Dunnen
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