| Human Disease |
Hypertrichosis, Congenital Generalized; HTC2 OMIM ID: 307150 |
| Synonyms | Cgh; Chromosome Xq27.1 Interchromosomal Insertion Syndrome; Hcg |
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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 05/22/2013 MGI 5.13 |
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