Term Name: glucocorticoid deficiency 4 with or without mineralocorticoid deficiency
Synonyms:
Definition: A familial glucocorticoid deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NNT gene on chromosome 5p12.
Ontology: Human Disease [DOID:0061243]   ( DOID:0061243 )

Relationships
is a type of: autosomal recessive disease familial glucocorticoid deficiency