Disease #01930 (ML-3 (mucolipidosis, type III, alpha/beta (ML-3, pseudo-Hurler polydystrophy)), OMIM:252600)

Official abbreviation ML-3
Name mucolipidosis, type III, alpha/beta (ML-3, pseudo-Hurler polydystrophy)
OMIM ID 252600
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GNPTAB
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Disease features -
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Individuals

1 entry on 1 page. Showing entry 1.
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00165049 GM01494 Journal: Kudo 2006 Unaffected heterozygous carrier parents. M ? United States - - 0 - - ML-3 - GNPTAB GNPTAB 1 1 Renata Voltolini Velho
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