Painless fractures due to injury
Symptom Information:
Symptom ID: | HPO:0002661 | ||
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal physiology(HPO:0011843) Increased susceptibility to fractures(HPO:0002659) Painless fractures due to injury(HPO:0002661) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
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All diseases associated with this symptom:
Channelopathy-associated congenital insensitivity to pain | (Orphanet:88642) |
Hereditary sensory and autonomic neuropathy type 2 | (Orphanet:970) |
Hereditary sensory and autonomic neuropathy type 5 | (Orphanet:64752) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA | (OMIM:201300) |
Navajo neurohepatopathy | (Orphanet:255229) |