DISEASES

Disease-gene associations mined from literature

Human genes for hypophosphatasia

Hypophosphatasia [DOID:14213]

A syndrome characterized by disruption of mineralization of bones and teeth that has_material_basis_in mutation in ALPL on chromosome 1p36.12.

Synonyms:  hypophosphatasia,  DOID:14213,  hypophosphatasias,  deficiency of alkaline phosphatase,  hypophospatasia, childhood ...

Linkouts:  OMIM #1 #2 #3