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Human Disease and Mouse Model Detail
Human Disease Hypertrichosis, Congenital Generalized, with or without Gingival Hyperplasia;
OMIM ID: 135400
Synonyms Chromosome 17q24.2-Q24.3 Deletion Syndrome; Chromosome 17q24.2-Q24.3 Duplication Syndrome; Fibromatosis, Gingival, with Hypertrichosis; Htc3; Hypertrichosis; Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia; Microdeletion 17q24.2-Q24.3 Syndrome; Microduplication 17q24.2-Q24.3 Syndrome
Genes and
mouse models
There are currently no human or mouse genes associated with this disease in the MGI database.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.03
The Jackson Laboratory