Phenotypes associated with the disease diabetes mellitus, transient neonatal, 1 (OMIM:601410, an entry in Online Mendelian Inheritance in Man):
- Transient neonatal diabetes mellitus (HP:0008255, a Human Phenotype Ontology term). Evidence: IEA. (OMIM:601410)
- Dehydration (HP:0001944, a Human Phenotype Ontology term). Evidence: IEA. (OMIM:601410)
- Severe failure to thrive (HP:0001525, a Human Phenotype Ontology term). Evidence: IEA. (OMIM:601410)
- Hyperglycemia (HP:0003074, a Human Phenotype Ontology term): An increased concentration of glucose in the blood. Evidence: IEA. (OMIM:601410)
- Intrauterine growth retardation (HP:0001511, a Human Phenotype Ontology term): An abnormal restriction of fetal growth with fetal weight below the tenth percentile for gestational age. Evidence: IEA. (OMIM:601410)
- Autosomal dominant inheritance (HP:0000006, a Human Phenotype Ontology term): A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele. Evidence: IEA. (OMIM:601410)