U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

CMDR Craniometaphyseal dysplasia, autosomal recessive [ Homo sapiens (human) ]

Gene ID: 64588, discontinued on 17-May-2014

Summary

Go to the top of the page Help
Gene symbol
CMDR
Gene description
Craniometaphyseal dysplasia, autosomal recessive
Primary source
MIM:218400
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

Go to the top of the page Help
Location:
6q21-q22

Bibliography

Go to the top of the pageHelp

GeneRIFs: Gene References Into Functions

Phenotypes

Go to the top of the page Help
Craniometaphyseal dysplasia, autosomal recessive

General gene information

Go to the top of the page Help

Markers

Property

  • phenotype only

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.