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Permanent neonatal diabetes mellitus
1 OMIM reference -
5 associated genes
49 connected diseases
No signs/symptoms info
Disease Type of connection
MODY syndrome
Transient neonatal diabetes mellitus
Hyperinsulinism due to glucokinase deficiency
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
Autosomal dominant hyperinsulinism due to SUR1 deficiency
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency
Autosomal recessive hyperinsulinism due to SUR1 deficiency
DEND syndrome
Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency
Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency
Partial pancreatic agenesis
Precursor B-cell acute lymphoblastic leukemia
Familial retinal arterial macroaneurysm
Familial retinoblastoma
Monosomy 13q14
Unilateral retinoblastoma
ALK-positive anaplastic large cell lymphoma
ALK-positive large B-cell lymphoma
Congenital stromal corneal dystrophy
Inflammatory myofibroblastic tumor
Neuroblastoma
Donnai-Barrow syndrome
Hyperinsulinism due to INSR deficiency
Insulin-resistance syndrome type A
Leprechaunism
Rabson-Mendenhall syndrome
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Distal hereditary motor neuropathy type 2
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
CLN10 disease
Autosomal agammaglobulinemia
Cataract-microcornea syndrome
Glycogen storage disease due to GLUT2 deficiency
Growth delay due to insulin-like growth factor I resistance
Melanoma of soft part
Nuclear cataract
Pulverulent cataract
Severe combined immunodeficiency due to DNA-PKcs deficiency
Alpha-crystallinopathy
Familial isolated dilated cardiomyopathy
Fatal infantile hypertonic myofibrillar myopathy
Posterior polar cataract
Zonular cataract
Synonym(s):
- PNDM
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
- Certain conditions originating in the perinatal period -
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.