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Ovarioleukodystrophy
1 OMIM reference -
5 associated genes
29 connected diseases
No signs/symptoms info
Disease Type of connection
Cree leukoencephalopathy
Familial congenital mirror movements
Giant cell glioblastoma
Gliosarcoma
Ataxia-telangiectasia-like disorder
Hereditary breast and ovarian cancer syndrome
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
Benign adult familial myoclonic epilepsy
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Peutz-Jeghers syndrome
Amyotrophic lateral sclerosis
Behavioral variant of frontotemporal dementia
Frontotemporal dementia with motor neuron disease
Hereditary sensory and autonomic neuropathy type 2
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Papillary or follicular thyroid carcinoma
Progressive non-fluent aphasia
Pseudohypoaldosteronism type 2C
Semantic dementia
Smith-Magenis syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.