Phenotype Details
Phene ID
3556
Name
Haplotype with homozygous deficiency BH1
Phene Name
N/A
OMIA ID
1825
Species ID
9913
Characterised
No
Characterised Year
N/A
Molecular Genetics

In an extensive study involving exome capture and next-gen sequencing, McClure et al. (2014) were not able to discover any potentially causal variant for haplotype BH1.

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