DISEASES

Disease-gene associations mined from literature

Human genes for Pelger-Huet anomaly

Pelger-Huet anomaly [DOID:9631]

Pelger-Huet anomaly is a blood laminopathy associated with the lamin B receptor.

Synonyms:  Pelger-Huet anomaly,  DOID:9631,  PelgerHuet anomaly

Linkouts:  OMIM