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URL: https://omim.org/clinicalSynopsis/105500


#105500
Table of Contents

AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1


Neuro
- Amyotrophic lateral sclerosis [SNOMEDCT: 86044005] [ICD10CM: G12.21] [ICD9CM: 335.20] [UMLS: C0002736 HPO: HP:0007354] [HPO: HP:0007354]
- Parkinsonism-dementia
- Progressive motor function loss
- Lower motor neuron manifestations [UMLS: C1865412 HPO: HP:0002366] [HPO: HP:0002366]
- Bulbar paralysis [SNOMEDCT: 54304004] [ICD10CM: G12.22] [ICD9CM: 335.22] [UMLS: C4082299, C0030442 HPO: HP:0001283]
Muscle
- Muscle weakness [SNOMEDCT: 26544005] [UMLS: C0030552, C0151786 HPO: HP:0001324] [HPO: HP:0001324]
- Muscle cramps [SNOMEDCT: 45352006, 55300003] [ICD10CM: M62.83] [ICD9CM: 728.85] [UMLS: C0026821, C0037763 HPO: HP:0003394] [HPO: HP:0003394]
Misc
- Chronic, progressive, and fatal [SNOMEDCT: 90734009] [UMLS: C1547296, C1555457, C0205191 HPO: HP:0011010] [HPO: HP:0011010]
Inheritance
- Autosomal dominant [SNOMEDCT: 771269000, 263681008] [UMLS: C0443147, C1867440 HPO: HP:0000006] [HPO: HP:0000006]

Creation Date:
Undefined
Edit History:
joanna : 05/05/2015

# 105500

AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1


SNOMEDCT: 838276009;   ORPHA: 90020;   DO: 0111246;   MONDO: 0007104;  


Neuro
- Amyotrophic lateral sclerosis [SNOMEDCT: 86044005] [ICD10CM: G12.21] [ICD9CM: 335.20] [UMLS: C0002736 HPO: HP:0007354] [HPO: HP:0007354]
- Parkinsonism-dementia
- Progressive motor function loss
- Lower motor neuron manifestations [UMLS: C1865412 HPO: HP:0002366] [HPO: HP:0002366]
- Bulbar paralysis [SNOMEDCT: 54304004] [ICD10CM: G12.22] [ICD9CM: 335.22] [UMLS: C4082299, C0030442 HPO: HP:0001283]
Muscle
- Muscle weakness [SNOMEDCT: 26544005] [UMLS: C0030552, C0151786 HPO: HP:0001324] [HPO: HP:0001324]
- Muscle cramps [SNOMEDCT: 45352006, 55300003] [ICD10CM: M62.83] [ICD9CM: 728.85] [UMLS: C0026821, C0037763 HPO: HP:0003394] [HPO: HP:0003394]
Misc
- Chronic, progressive, and fatal [SNOMEDCT: 90734009] [UMLS: C1547296, C1555457, C0205191 HPO: HP:0011010] [HPO: HP:0011010]
Inheritance
- Autosomal dominant [SNOMEDCT: 771269000, 263681008] [UMLS: C0443147, C1867440 HPO: HP:0000006] [HPO: HP:0000006]

Creation Date:
Undefined

Edit History:
joanna : 05/05/2015



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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2026 Johns Hopkins University.
NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2026 Johns Hopkins University.
Printed: April 5, 2026