Details of Disease

General Information of Disease (ID: DIS25HMJ)

Disease Name Alternating hemiplegia
Disease Hierarchy
DIS372XH: Neurodevelopmental disorder
DIS25HMJ: Alternating hemiplegia
Disease Identifiers
MONDO ID
MONDO_0016210
MESH ID
D006429
UMLS CUI
C0278110
MedGen ID
124456
Orphanet ID
209978
SNOMED CT ID
404689008

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 2 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
CGA TTFC29G Strong Biomarker [1]
SLC1A3 TT8WRDA Strong Genetic Variation [2]
------------------------------------------------------------------------------------
This Disease Is Related to 2 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
ATP1A3 OTM8EG6H Strong Genetic Variation [3]
TBC1D24 OTKZUSMD Definitive Genetic Variation [4]
------------------------------------------------------------------------------------

References

1 Hemiplegia after thyrotropin alfa in a hypothyroid patient with thyroid carcinoma metastatic to the brain.J Clin Endocrinol Metab. 1999 Nov;84(11):3867-71. doi: 10.1210/jcem.84.11.6161.
2 Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake. Arch Neurol. 2009 Jan;66(1):97-101. doi: 10.1001/archneurol.2008.535.
3 Alternating hemiplegia of childhood and a pathogenic variant of ATP1A3: a case report and pathophysiological considerations.Epileptic Disord. 2017 Jun 1;19(2):226-230. doi: 10.1684/epd.2017.0913.
4 Alternating Hemiplegia and Epilepsia Partialis Continua: A new phenotype for a novel compound TBC1D24 mutation.Seizure. 2017 Apr;47:71-73. doi: 10.1016/j.seizure.2017.03.003. Epub 2017 Mar 6.