Mitten deformity
Symptom Information:
Symptom ID: | HPO:0004057 | |||
Synonyms: |
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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 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 upper limb(HPO:0002817) Abnormality of the hand(HPO:0001155) Abnormal hand morphology(HPO:0005922) Mitten deformity(HPO:0004057) MedDRA: |
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Database Frequency: | 3 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Lethal acantholytic epidermolysis bullosa | (Orphanet:158687) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |