Disease #01932 (ML4 (Mucolipidosis IV), OMIM:252650)

Official abbreviation ML4
Name Mucolipidosis IV
OMIM ID 252650
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 MCOLN1
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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00466473 - - - M yes Morocco - - - - - ML4 Vitreoretinopathy, Delayed speech and language development, Hearing impairment, Hypotonia, Motor delay, achlorhydria, anaemia, MCOLN1 MCOLN1 1 1 Maria Elena García Paya
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