Osteomyelitis or necrosis, distal, due to sensory neuropathy (feet)

Symptom Information:

Symptom ID: HPO:0001886
Synonyms:
Osteomyelitis or necrosis, distal, due to sensory neuropathy [OMIM:Osteomyelitis or necrosis, distal, due to sensory neuropathy]
Quality:
Cross references:
OMIM: "Osteomyelitis or necrosis, distal, due to sensory neuropathy" [OMIM:Osteomyelitis or necrosis, distal, due to sensory neuropathy]
Is a (Direct Parents):
HPO         Sensory neuropathy
HPO         Abnormality of the foot
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 neuropathy(HPO:0000763)
                      Osteomyelitis or necrosis, distal, due to sensory neuropathy (feet)(HPO:0001886)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of the foot(HPO:0001760)
                         Osteomyelitis or necrosis, distal, due to sensory neuropathy (feet)(HPO:0001886)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Charcot-Marie-Tooth disease type 2B (Orphanet:99936)
Hereditary sensory and autonomic neuropathy type 1 (Orphanet:36386)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA (OMIM:162400)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC (OMIM:613640)
NEUROPATHY, HEREDITARY SENSORY, TYPE ID (OMIM:613708)