Hsd10 Disease, Atypical Type

Clinical Features

Phenotypes and symptoms related to Hsd10 Disease, Atypical Type

  • Intellectual disability
  • Behavioral abnormality
  • Abnormality of movement

Incidence and onset information

Not enough data available about incidence and published cases.
No data available about the known clinical features onset.

Alternative names

Hsd10 Disease, Atypical Type Is also known as syndromic x-linked intellectual disability type 10, hsd10 deficiency, atypical type, x-linked intellectual disability-choreoathetosis-abnormal behavior syndrome.

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.


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Hsd10 Disease, Atypical Type Recommended genes panels

Panel Name, Specifity and genes Tested/covered
MitoMetĀ®Plus aCGH Analysis.

By Baylor Miraca Genetics Laboratories (United States).

RGS9, RHO, GRK1, RLBP1, RNASEL, BCS1L, RP1, RP2, RP9, RPE65, RPGR, RPL35A, MRPL3, RPS14, RS1, SAG, SARDH, SCO2, SCP2, SDHB , (...)

View the complete list with 612 more genes
Specificity
1 %
Genes
100 %
HSD17B10 Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories (United States).

HSD17B10
Specificity
100 %
Genes
100 %
HSD17B10 Familial Mutation/Variant Analysis.

By Baylor Miraca Genetics Laboratories (United States).

HSD17B10
Specificity
100 %
Genes
100 %
HSD17B10 Prenatal Sequence Analysis.

By Baylor Miraca Genetics Laboratories (United States).

HSD17B10
Specificity
100 %
Genes
100 %
HSD17B10 Sequence & Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories (United States).

HSD17B10
Specificity
100 %
Genes
100 %
HSD17B10 Sequence Analysis.

By Baylor Miraca Genetics Laboratories (United States).

HSD17B10
Specificity
100 %
Genes
100 %
Epilepsy Advanced Sequencing and CNV Evaluation.

By Athena Diagnostics Inc (United States).

SCN1A, SCN1B, SCN2A, SCN3A, SCN5A, SCN8A, SCN9A, SHH, ST3GAL3, ST3GAL5, STIL, SIX3, SLC2A1, SLC35A2, SLC6A1, SLC6A8, SLC9A6, SMC1A, KDM5C, SMS , (...)

View the complete list with 214 more genes
Specificity
1 %
Genes
100 %
Epilepsy Advanced Sequencing and CNV Evaluation - Intellectual Disability.

By Athena Diagnostics Inc (United States).

SLC35A2, SLC6A8, SLC9A6, SMC1A, KDM5C, SMS, SNAP25, CDKL5, SYN1, SYP, CACNA2D1, PCDH19, ARHGEF9, DEAF1, CASK, ALG9, RAB39B, BCKDK, ARX, SPATA5 , (...)

View the complete list with 36 more genes
Specificity
2 %
Genes
100 %

We have 59 more panels available in our App

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Sources and references

You can check the following sources for additional information.

MESH ORPHANET Genetic Syndrome Finder

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