Clinical Signs and Symptoms
ORPHA:99885 Permanent neonatal diabetes mellitus
The phenotypic description of this disease is based on an analysis of the biomedical literature and uses the terms of the Human Phenotype Ontology (HPO). Phenotypic abnormalities are presented by order of frequency of occurrence in the patient population, then by alphabetical order inside each frequency group.
- Abnormal heart morphology HP:0001627
- Arthrogryposis multiplex congenita HP:0002804
- Bilateral ptosis HP:0001488
- Contractures of the joints of the lower limbs HP:0005750
- Downturned corners of mouth HP:0002714
- Generalized myoclonic seizures HP:0002123
- Generalized tonic-clonic seizures HP:0002069
- Global developmental delay HP:0001263
- Intellectual disability HP:0001249
- Intrauterine growth retardation HP:0001511
- Ketonuria HP:0002919
- Microalbuminuria HP:0012594
- Motor delay HP:0001270
- Neurodevelopmental delay HP:0012758
- Polyuria HP:0000103
- Prominent metopic ridge HP:0005487
- Retinopathy HP:0000488
- Abnormality of the upper urinary tract HP:0010935
- Apraxia HP:0002186
- Ataxia HP:0001251
- Coma HP:0001259
- Hearing impairment HP:0000365
- Intellectual disability, severe HP:0010864
- Muscular hypotonia HP:0001252
- Pancreatic hypoplasia HP:0002594
- Peripheral axonal neuropathy HP:0003477
- Renal tubular dysfunction HP:0000124
- Autoimmune antibody positivity HP:0030057
Specialised Social Services
The information provided is based on published scientific articles.
The information provided is estimated for the entire population of patients in routine care. Some phenotypic abnormalities reported here may occur individually with a variable temporality or severity, while others, not listed, may still be encountered. Phenotypic annotations are not yet available for all rare diseases; the annotation process is ongoing.
The information contained in Orphanet is regularly updated. It is possible that discoveries have been made since the last update and have not yet been incorporated.
Professionals are encouraged to always consult the latest scientific publications before making a decision based on the information provided. The information contained in Orphanet is not intended to replace the services of a healthcare professional. Orphanet cannot be held responsible for the deleterious, truncated or erroneous use of any information found in the Orphanet database.