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Transient neonatal diabetes mellitus

3 OMIM references -
5 associated genes
31 connected diseases
No signs/symptoms info

Disease	Type of connection
MODY syndrome
Permanent neonatal diabetes mellitus
Paternal uniparental disomy of chromosome 6
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
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Essential thrombocythemia
Familial pancreatic carcinoma
Giant cell glioblastoma
Gliosarcoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Precursor B-cell acute lymphoblastic leukemia
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Aneurysm - osteoarthritis syndrome
Cerebellar ataxia-deafness-narcolepsy syndrome
Familial thoracic aortic aneurysm and aortic dissection
ICF syndrome
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Acute promyelocytic leukemia
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Cataract-microcornea syndrome
Nuclear cataract
Pulverulent cataract

Synonym(s): - TNDM

Classification (Orphanet): - Rare endocrine disease - Rare genetic disease		Classification (ICD10): - Certain conditions originating in the perinatal period -

Epidemiological data: (no data available)		External references: 3 OMIM references - No MeSH references

No signs/symptoms info available.