disease has basis in dysfunction of TMEM67 Meckel syndrome, type 3 Any Meckel syndrome in which the cause of the disease is a mutation in the TMEM67 gene. DOID:0070117 GARD:0008744 ICD10:Q61.9 MESH:C536132 MKS3 MONDO:0011821 Meckel syndrome 3 Meckel syndrome caused by mutation in TMEM67 Meckel syndrome type 3 Meckel syndrome, type 3 Meckel-Gruber syndrome, type 3 OMIM:607361 TMEM67 Meckel syndrome UMLS:C1846357 https://rarediseases.info.nih.gov/diseases/8744/meckel-syndrome-type-3 Meckel syndrome