Human genes for Laron syndrome
Laron syndrome [DOID:9521]
A syndrome characterized by marked short stature with normal or high serum growth hormone and low serum insulin-like growth factor-1 levels that has_material_basis_in homozygous or compound heterozygous mutation in GHR on chromosome 5p13-p12.
Synonyms: Laron syndrome, DOID:9521, Laron disease, Laron disorder, Laron syndromes ...
Linkouts: OMIM