| Human Disease |
Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia OMIM ID: 135400 |
| Synonyms | Chromosome 17q24.2-Q24.3 Deletion Syndrome; Fibromatosis, Gingival, with Hypertrichosis; Microdeletion 17q24.2-Q24.3 Syndrome |
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Genes and mouse models |
There are currently no human or mouse genes associated with this disease in the MGI database. |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/12/2013 MGI 5.14 |
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