Autoamputation
Symptom Information:
Symptom ID: | HPO:0001218 | |||||||||||||||
Synonyms: |
|
|||||||||||||||
Quality: | ||||||||||||||||
Cross references: |
|
|||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) 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) Autoamputation(HPO:0001218) MedDRA: |
|||||||||||||||
Database Frequency: | 10 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2B | (Orphanet:99936) |
Classical phenylketonuria | (Orphanet:79254) |
Dopa-responsive dystonia due to sepiapterin reductase deficiency | (Orphanet:70594) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Keratoderma hereditarium mutilans | (Orphanet:494) |
Maternal hyperphenylalaninemia | (Orphanet:2209) |
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) |
Phenylketonuria | (Orphanet:716) |