has characteristic has characteristic has material basis in germline mutation in GLIS3 neonatal diabetes mellitus with congenital hypothyroidism https://github.com/monarch-initiative/mondo/issues/4069 https://www.malacards.org/card/diabetes_mellitus_neonatal_with_congenital_hypothyroidism UMLS:C1857775 NDH DOID:0060638 MONDO:0012436 OMIM:610199 MESH:C565705 GARD:0016699 MEDGEN:347541 NDH syndrome A rare genetic disease characterized by intrauterine growth retardation, permanent neonatal diabetes mellitus, and congenital hypothyroidism. Additional manifestations include congenital glaucoma, hepatic disease (hepatitis, fibrosis, and cirrhosis), polycystic kidneys, exocrine pancreatic dysfunction, sensorineural hearing impairment, developmental delay, and mild facial dysmorphism (such as flat nasal bridge, epicanthal folds, long philtrum, and low-set ears), among others neonatal diabetes mellitus with congenital hypothyroidism Orphanet:79118 neonatal diabetes mellitus familial cystic renal disease congenital