Disease #03334 (ALS12 (sclerosis, lateral, amyotrophic, type type 12 (ALS12)), OMIM:613435)

Official abbreviation ALS12
Name sclerosis, lateral, amyotrophic, type type 12 (ALS12)
OMIM ID 613435
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene OPTN
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Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00397528 190239 - - M no Germany - - - - - ALS12 Skeletal muscle atrophy, Muscle weakness, Proximal muscle weakness, Elevated circulating creatine kinase concentration, Polyneuropathy, Sensory axonal neuropathy, Peripheral axonal neuropathy, Peripheral neuropathy, Calcium channel antibody positivity, Autoimmunity ; father with ALS HEXA, OPTN HEXA, OPTN 3 1 Andreas Laner
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