|Name||Wolf-Hirschhorn syndrome chromosome region|
|Description||Wolf-Hirschhorn syndrome is a congenital malformation syndrome characterized by pre- and postnatal growth deficiency, developmental disability of variable degree, characteristic craniofacial features ('Greek warrior helmet' appearance of the nose, high forehead, prominent glabella, hypertelorism, high-arched eyebrows, protruding eyes, epicanthal folds, short philtrum, distinct mouth with downturned corners, and micrognathia), and a seizure disorder (Battaglia et al., 2008 [PubMed 18932224]).[supplied by OMIM, Nov 2010]|
|NCBI Gene ID||7467|
|Expression in Tissues and Cell Lines||
WHCR has 1 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 1 datasets.
Click the + buttons to view associations for WHCR from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with WHCR gene/protein from the curated CTD Gene-Disease Associations dataset.|