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Medulloblastoma with extensive nodularity
1 OMIM reference -
1 associated gene
26 connected diseases
No signs/symptoms info
Disease Type of connection
Desmoplastic / nodular medulloblastoma
Familial multiple meningioma
Neonatal diabetes - congenital hypothyroidism - congenital glaucoma - hepatic fibrosis - polycystic kidneys
Infantile Refsum disease
Neonatal adrenoleukodystrophy
Zellweger syndrome
Acrocallosal syndrome
Alobar holoprosencephaly
Combined pituitary hormone deficiencies, genetic forms
Greig cephalopolysyndactyly syndrome
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Pallister-Hall syndrome
Polysyndactyly, bilateral
Polysyndactyly, unilateral
Postaxial polydactyly type A, bilateral
Postaxial polydactyly type A, unilateral
Postaxial polydactyly type B, bilateral
Postaxial polydactyly type B, unilateral
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Amyotrophic lateral sclerosis
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Split hand-split foot malformation
Adams-Oliver syndrome
Synonym(s):
- Cerebellar neuroblastoma
Classification (Orphanet):
- Rare neurologic disease
- Rare oncologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: sporadic
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SUFU Q9UMX1607035
No signs/symptoms info available.