Disease #01032 (AMD2C (dysplasia, acromesomelic, type 2C, Hunter-Thompson), OMIM:201250)

Official abbreviation AMD2C
Name dysplasia, acromesomelic, type 2C, Hunter-Thompson
OMIM ID 201250
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene GDF5
Associated tissues -
Disease features -
Remarks -