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Feingold syndrome type 1
1 OMIM reference -
1 associated gene
14 connected diseases
No signs/symptoms info
Disease Type of connection
Neuroblastoma
Hereditary pheochromocytoma-paraganglioma
Autosomal recessive limb-girdle muscular dystrophy type 2H
Bardet-Biedl syndrome
Familial medullary thyroid carcinoma
Familial melanoma
Familial pancreatic carcinoma
Hereditary sensory and autonomic neuropathy type 4
Hereditary sensory and autonomic neuropathy type 5
Melanoma and neural system tumor syndrome
Melanoma-pancreatic cancer syndrome
Papillary or follicular thyroid carcinoma
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Synonym(s):
- Brunner-Winter syndrome type 1
- Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1
- FGLDS1
- FS1
- MMT type 1
- MODED syndrome type 1
- Microcephaly - intellectual deficit - tracheoesophageal fistula type 1
- Microcephaly - oculo-digito-esophageal-duodenal syndrome type 1
- Microcephaly-digital anomalies-normal intelligence type 1
- ODED syndrome type 1
- Oculo-digito-esophageal-duodenal syndrome type 1
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: adult
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
MYCN P04198164840
No signs/symptoms info available.