| Disease Aliases (117) | Asymbolia for pain Acroosteolyses, neurogenic Acroosteolysis, giaccai type Acroosteolysis, neurogenic Analgesia, congenital Asymbolia Cip Congenital analgesia, autosomal recessive Channelopathy-associated insensitivity to pain Channelopathy-associated cip Channelopathy-associated congenital insensitivity to pain Congenital analgesia Congenital indifference to pain Congenital insensitivity to pain Congenital insensitivity to pain with anhidrosis Congenital pain indifference Congenital pain indifferences Congenital pain insensitivity Congenital sensory neuropathies Congenital insensitivity to pain and thermal analgesia Congenital pain asymbolia Congenital sensory neuropathy with selective loss of small myelinated fibers Familial dysautonomia, type 2 Familial dysautonomia, type ii Giaccai type acroosteolysis Hsan Hsan (hereditary sensory autonomic neuropathy) Hsan - hereditary sensory and autonomic neuropathy Hsan 1 Hsan 4 Hsan 5 Hsan i Hsan iv Hsan type i Hsan type ii Hsan type iv Hsan type v Hsan v Hsan2 Hsan2d Hsan2d, ar Hsan5 Hsanii Hsans (hereditary sensory autonomic neuropathy) Hsn type i Hsn type ii Hsn type iis Hereditary sensory and autonomic neuropathy iv Hereditary sensory autonomic neuropathy, type 1 Hereditary sensory autonomic neuropathy, type 2 Hereditary sensory autonomic neuropathy, type 4 Hereditary sensory autonomic neuropathy, type 5 Hereditary sensory neuropathies Hereditary sensory neuropathy Hereditary sensory neuropathy type 1 Hereditary sensory neuropathy type i Hereditary sensory neuropathy type ia Hereditary sensory radicular neuropathy Hereditary sensory radicular neuropathy, recessive form Hereditary sensory and autonomic neuropathies Hereditary sensory and autonomic neuropathy 4 Hereditary sensory and autonomic neuropathy type 1 Hereditary sensory and autonomic neuropathy type 2 Hereditary sensory and autonomic neuropathy type i Hereditary sensory and autonomic neuropathy type ii Hereditary sensory and autonomic neuropathy type iv Hereditary sensory and autonomic neuropathy type v Hereditary sensory and autonomic neuropathy, type 4 Hereditary sensory and autonomic neuropathy, type 5 Hereditary sensory and autonomic neuropathy Hereditary sensory and autonomic neuropathy type 5 Hereditary sensory and autonomic neuropathy, type v Hereditary sensory autonomic neuropathy Insensitivity to pain, channelopathy-associated Insensitivity to pain, congenital Insensitivity to pain with anhidrosis, congenital Insensitivity to pain, congenital, with anhidrosis Insensitivity, congenital pain Neuropathy, hereditary sensory and autonomic, type iid Ngf autosomal recessive hereditary sensory and autonomic neuropathy Neurogenic acroosteolyses Neurogenic acroosteolysis Neuropathies, congenital sensory Neuropathies, hereditary sensory Neuropathies, hereditary sensory and autonomic Neuropathy hereditary sensory radicular, autosomal dominant Neuropathy hereditary sensory and autonomic type 1 Neuropathy, congenital sensory Neuropathy, congenital sensory, with anhidrosis Neuropathy, hereditary sensory Neuropathy, hereditary sensory and autonomic, type i Neuropathy, hereditary sensory and autonomic, type v Neuropathy, hereditary sensory radicular, autosomal dominant Neuropathy, hereditary sensory radicular, autosomal recessive Neuropathy, hereditary sensory, type i Neuropathy, progressive sensory, of children Pain indifference, congenital Pain insensitivity with anhidrosis, congenital Pain insensitivity, congenital Scn9a-related congenital insensitivity to pain Sensory neuropathies, congenital Sensory neuropathies, hereditary Sensory neuropathy, congenital Sensory neuropathy, hereditary Sensory and autonomic neuropathies, hereditary Type i, hsan Type i, hsn Type iv, hsan Autosomal recessive hereditary sensory and autonomic neuropathy caused by mutation in ngf Channelopathy-associated congenital insensitivity to pain, autosomal recessive Hereditary sensory peripheral neuropathy Indifference to pain, congenital, autosomal recessive Indifference to pain, congenital, autosomal recessive; cip Neuropathy, hereditary sensory and autonomic, type 2d Neuropathy, hereditary sensory and autonomic, type 5 Neuropathy, hereditary sensory and autonomic, type v; hsan5 |
Associated Genes (3) NCBI-RefSeq: SCN9A (Sodium voltage-gated channel alpha subunit 9) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: SCN11A (Sodium voltage-gated channel alpha subunit 11) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: SCN10A (Sodium voltage-gated channel alpha subunit 10) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Congenital sensory neuropathy with selective loss of small myelinated fibers | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |