Pain insensitivity
Symptom Information:
Symptom ID: | HPO:0007021 | ||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Abnormal peripheral nervous system morphology(HPO:0000759) Peripheral neuropathy(HPO:0009830) Sensory impairment(HPO:0003474) Abnormality of pain sensation(HPO:0010832) Impaired pain sensation(HPO:0007328) Pain insensitivity(HPO:0007021) MedDRA: |
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Database Frequency: | 35 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
16p11.2p12.2 microdeletion syndrome | (Orphanet:261211) |
2q37 microdeletion syndrome | (Orphanet:1001) |
Autosomal dominant cerebellar ataxia | (Orphanet:99) |
Autosomal dominant optic atrophy plus syndrome | (Orphanet:1215) |
Channelopathy-associated congenital insensitivity to pain | (Orphanet:88642) |
Charcot-Marie-Tooth disease | (Orphanet:166) |
Down syndrome | (Orphanet:870) |
Familial dysautonomia | (Orphanet:1764) |
Flynn-Aird syndrome | (Orphanet:2047) |
Gemignani syndrome | (Orphanet:2074) |
Gómez-López-Hernández syndrome | (Orphanet:1532) |
Hemihypertrophy | (Orphanet:2128) |
Hereditary sensory and autonomic neuropathy type 4 | (Orphanet:642) |
Hereditary sensory and autonomic neuropathy type 5 | (Orphanet:64752) |
Hereditary sensory and autonomic neuropathy with spastic paraplegia | (Orphanet:139578) |
Hereditary spastic paraplegia | (Orphanet:685) |
INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL DOMINANT | (OMIM:147430) |
INSENSITIVITY TO PAIN WITH HYPERPLASTIC MYELINOPATHY | (OMIM:147530) |
Infantile axonal neuropathy | (Orphanet:2679) |
Monosomy 22q13 | (Orphanet:48652) |
Myalgia-eosinophilia syndrome associated with tryptophan | (Orphanet:2582) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII | (OMIM:615548) |
Navajo neurohepatopathy | (Orphanet:255229) |
Polyneuropathy - hand defect | (Orphanet:2926) |
Smith-Magenis syndrome | (Orphanet:819) |
Spastic paraparesis - deafness | (Orphanet:2815) |
Stiff skin syndrome | (Orphanet:2833) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
Tangier disease | (Orphanet:31150) |
Van Regemorter-Pierquin-Vamos syndrome | (Orphanet:3419) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |
X-linked Charcot-Marie-Tooth disease type 2 | (Orphanet:101076) |
X-linked Charcot-Marie-Tooth disease type 3 | (Orphanet:101077) |
X-linked Charcot-Marie-Tooth disease type 4 | (Orphanet:101078) |
X-linked Charcot-Marie-Tooth disease type 5 | (Orphanet:99014) |