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Amyotrophic lateral sclerosis-parkinsonism-dementia complex
1 OMIM reference -
2 associated genes
63 connected diseases
No signs/symptoms info
Disease Type of connection
Young adult-onset Parkinsonism
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Translocation renal cell carcinoma
Bardet-Biedl syndrome
Bannayan-Riley-Ruvalcaba syndrome
Complete androgen insensitivity syndrome
Cowden syndrome
Early infantile epileptic encephalopathy
Familial hypospadias
Hereditary breast and ovarian cancer syndrome
Juvenile polyposis of infancy
Kennedy disease
Lhermitte-Duclos disease
Macrocephaly-autism syndrome
Malignant migrating partial seizures of infancy
Partial androgen insensitivity syndrome
Proteus syndrome
Proteus-like syndrome
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus
Squamous cell carcinoma of head and neck
FADD-related immunodeficiency
Oculootodental syndrome
Parkinsonian-pyramidal syndrome
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome
Brain dopamine-serotonin vesicular transport disease
Isolated cytochrome C oxidase deficiency
Precursor B-cell acute lymphoblastic leukemia
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Acute promyelocytic leukemia
Adrenocortical carcinoma
Amyotrophic lateral sclerosis
Autosomal dominant hypohidrotic ectodermal dysplasia
B-cell chronic lymphocytic leukemia
Cerebellar ataxia - hypogonadism
Chuvash erythrocytosis
Cold-induced sweating syndrome
Epilepsy with myoclonic-astatic seizures
Essential thrombocythemia
Familial pancreatic carcinoma
Fanconi anemia
Giant cell glioblastoma
Gliosarcoma
Isolated NADH-CoQ reductase deficiency
Leber hereditary optic neuropathy
Leigh syndrome with leukodystrophy
Lennox-Gastaut syndrome
Li-Fraumeni syndrome
MELAS syndrome
Maternally-inherited Leigh syndrome
Papilloma of choroid plexus
Von Hippel-Lindau disease
Autoimmune lymphoproliferative syndrome with recurrent infections
Primary hypomagnesemia with secondary hypocalcemia
Cataract-glaucoma
Familial ocular anterior segment mesenchymal dysgenesis
Posterior polar cataract
Spinocerebellar ataxia type 26
Transaldolase deficiency
Autosomal dominant Charcot-Marie-Tooth disease type 2A1
Chronic myeloid leukemia
Precursor T-cell acute lymphoblastic leukemia
Synonym(s):
- Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam
- Guam disease
- Lytico-Bodig disease
- PDALS
- Parkinsonism-dementia-ALS complex
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
PARK7 Q99497602533
TRPM7 Q96QT4605692
No signs/symptoms info available.