| Disease | MONDO ID | OMIM disease number | Causal gene | Inheritance | Common synonyms | Key supporting note |
|---|---|---|---|---|---|---|
| Mucolipidosis type IV | MONDO:0009653 | OMIM 252650 | MCOLN1 | Autosomal recessive (AR) | Mucolipidosis IV; MLIV | Open Targets lists the disease-target association for mucolipidosis type IV with MONDO_0009653 and MCOLN1; MLIV is described as an autosomal-recessive lysosomal disorder caused by MCOLN1/TRPML1 variants, and OMIM 252650 is explicitly referenced in MLIV literature (pqac-00000000, pqac-00000003, pqac-00000001) |


*Table: This table summarizes core standardized identifiers and naming conventions for mucolipidosis type IV, including its MONDO and OMIM identifiers, causal gene, inheritance pattern, and common synonyms. It is useful as a compact reference for disease knowledge base curation.*