Hydrocephalus (Version: )

Relevant disorders: Hydrocephalus, R86, GT719, TP187
Signed off date: 12 Aug 2026
Panel types: Rare Disease 100K, GMS Rare Disease Virtual, GMS signed-off
76 green entities
Entity ratingEntityMode of inheritanceMode of pathogenicityTags
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/Amosaicism, somatic
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X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)N/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)N/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownOtherN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalOtherfounder-effect
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X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)N/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/Anew-gene-name
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/Anew-gene-name
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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X-LINKED: hemizygous mutation in males, biallelic mutations in femalesN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/Asomatic
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownOtherN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)N/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, NOT imprintedN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/Anew-gene-name
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, NOT imprintedN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)N/AN/A
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BIALLELIC, autosomal or pseudoautosomalN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknownN/AN/A
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X-LINKED: hemizygous mutation in males, biallelic mutations in femalesN/AN/A