Madelung deformity
Symptom Information:
Symptom ID: | HPO:0003067 | |||||||||
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 upper limb joint(HPO:0009810) Abnormality of the wrist(HPO:0003019) Madelung deformity(HPO:0003067) Abnormal joint morphology(HPO:0001367) Abnormality of upper limb joint(HPO:0009810) Abnormality of the wrist(HPO:0003019) Madelung deformity(HPO:0003067) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396) Musculoskeletal and connective tissue disorders of limbs congenital(MedDRA:10028381) Madelung deformity(HPO:0003067) |
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Database Frequency: | 9 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
Brachydactyly type C | (Orphanet:93384) |
Dyschondrosteosis - nephritis | (Orphanet:1765) |
Langer mesomelic dysplasia | (Orphanet:2632) |
Léri-Weill dyschondrosteosis | (Orphanet:240) |
Madelung deformity | (Orphanet:35688) |
Microcephalic primordial dwarfism, Dauber type | (Orphanet:319675) |
Multiple osteochondromas | (Orphanet:321) |
Oculo-skeletal-renal syndrome | (Orphanet:2716) |
Oculodentodigital dysplasia | (Orphanet:2710) |