disease has basis in dysfunction of CA2 autosomal recessive osteopetrosis 3 Autosomal Recessive osteopetrosis, type 3 CA2 osteopetrosis (disease) DOID:0110941 GARD:0004154 Guibaud Vainsel syndrome Guibaud-Vainsel syndrome ICD10:Q78.2 ICD9:588.89 MESH:C536058 MONDO:0009818 NCIT:C118438 OMIM:259730 OPTB3 Orphanet:2785 Osteopetrosis with renal tubular acidosis is a rare disorder characterized by osteopetrosis, renal tubular acidosis (RTA), and neurological disorders related to cerebral calcifications. SCTID:254122007 autosomal recessive osteopetrosis 3 with renal tubular acidosis autosomal recessive osteopetrosis type 3 carbonic anhydrase 2 deficiency carbonic anhydrase II deficiency https://rarediseases.info.nih.gov/diseases/4154/osteopetrosis-autosomal-recessive-3 marble brain disease mixed RTA mixed renal tubular acidosis osteopetrosis (disease) caused by mutation in CA2 osteopetrosis autosomal recessive 3 osteopetrosis with renal tubular acidosis osteopetrosis, autosomal recessive 3 osteopetrosis, autosomal recessive type 3 renal tubular acidosis type 3 osteopetrosis (disease) primary renal tubular acidosis autosomal recessive osteopetrosis