DISEASES

Disease-gene associations mined from literature

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Human genes for craniodiaphyseal dysplasia

Craniodiaphyseal dysplasia [DOID:0080032]

An osteosclerosis that results_in increased calcium concentration located_in skull which decreases the size of cranium foramina and cervical spinal canal.

Synonyms:  craniodiaphyseal dysplasia,  DOID:0080032,  craniodiaphyseal dysplasias

Linkouts:  OMIM #1 #2

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.