Migraine, Familial Hemiplegic, 1; Fhm1

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Migraine, Familial Hemiplegic, 1; Fhm1

CACNA1A

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Migraine, Familial Hemiplegic, 1; Fhm1

Intellectual disability
Seizures
Global developmental delay
Generalized hypotonia
Hearing impairment
Ataxia
Nystagmus
Pain
Motor delay
Fever

And another 25 symptoms. If you need more information about this disease we can help you.

Click here to know more about Mendelian.

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Alternative names

Migraine, Familial Hemiplegic, 1; Fhm1 Is also known as mhp1, fhm.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Migraine, Familial Hemiplegic, 1; Fhm1 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
SCA6 (CACNA1A) Repeat Expansion Test. By Athena Diagnostics Inc (United States). CACNA1A Specificity 100 % Genes 100 %
Ataxia, Common Repeat Expansion Evaluation. By Athena Diagnostics Inc (United States). ATXN1, ATXN10, ATXN2, ATXN7, ATXN8OS, TBP, CACNA1A, ATXN3 Specificity 13 % Genes 100 %
Episodic Ataxia Evaluation. By Athena Diagnostics Inc (United States). SLC1A3, CACNA1A, CACNB4, KCNA1 Specificity 25 % Genes 100 %
Ataxia, Comprehensive Evaluation. By Athena Diagnostics Inc (United States). SACS, ATXN1, ATXN10, ATXN2, ATXN7, ATXN8OS, SLC1A3, SPTBN2, TBP, TTPA, VAMP1, CACNA1A, CACNB4, APTX, TGM6, COQ8A, SYNE1, TDP1, TTBK2, SYT14 , (...) View the complete list with 22 more genes Panel complete gene list SACS, ATXN1, ATXN10, ATXN2, ATXN7, ATXN8OS, SLC1A3, SPTBN2, TBP, TTPA, VAMP1, CACNA1A, CACNB4, APTX, TGM6, COQ8A, SYNE1, TDP1, TTBK2, SYT14, SIL1, FLVCR1, ANO10, MTPAP, ATN1, AFG3L2, EEF2, FGF14, FXN, SETX, GRM1, ITPR1, KCNA1, KCNC3, KCND3, ATXN3, MRE11, ATM, PDYN, POLG, PPP2R2B, PRKCG Specificity 3 % Genes 100 %
Ataxia, Supplemental Dominant Evaluation. By Athena Diagnostics Inc (United States). SLC1A3, SPTBN2, VAMP1, CACNA1A, CACNB4, TGM6, TTBK2, AFG3L2, EEF2, FGF14, ITPR1, KCNA1, KCNC3, KCND3, PDYN, PRKCG Specificity 7 % Genes 100 %
Ataxia, Complete Dominant Evaluation. By Athena Diagnostics Inc (United States). ATXN1, ATXN10, ATXN2, ATXN7, ATXN8OS, SLC1A3, SPTBN2, TBP, VAMP1, CACNA1A, CACNB4, TGM6, TTBK2, ATN1, AFG3L2, EEF2, FGF14, ITPR1, KCNA1, KCNC3 , (...) View the complete list with 5 more genes Panel complete gene list ATXN1, ATXN10, ATXN2, ATXN7, ATXN8OS, SLC1A3, SPTBN2, TBP, VAMP1, CACNA1A, CACNB4, TGM6, TTBK2, ATN1, AFG3L2, EEF2, FGF14, ITPR1, KCNA1, KCNC3, KCND3, ATXN3, PDYN, PPP2R2B, PRKCG Specificity 4 % Genes 100 %
Hemiplegic Migraine Sequencing Evaluation. By Athena Diagnostics Inc (United States). SCN1A, CACNA1A, ATP1A2 Specificity 34 % Genes 100 %
CACNA1A Sequencing Test. By Athena Diagnostics Inc (United States). CACNA1A Specificity 100 % Genes 100 %

You can get up to 156 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like NEUROFIBROMATOSIS-NOONAN SYNDROME GLYCEROL KINASE DEFICIENCY; GKD BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES MACULAR DEGENERATION, AGE-RELATED, 1; ARMD1 LISSENCEPHALY 3; LIS3 ATTENTION DEFICIT-HYPERACTIVITY DISORDER; ADHD