Abnormal morphology of bones of the upper limbs
Symptom Information:
| Symptom ID: | HPO:0040065 | ||||
| Synonyms: |
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| Cross references: |
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| Is a (Direct Parents): |
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| Is a (Whole tree): |
HPO:
MedDRA: |
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| Database Frequency: | 25 / 7739 | ||||
| Resource: | HPO |
All diseases associated with this symptom:
| Acheiropodia | (Orphanet:931) |
| Adams-Oliver syndrome | (Orphanet:974) |
| Amniotic bands | (Orphanet:1034) |
| CHILD syndrome | (Orphanet:139) |
| Dermatoosteolysis, Kirghizian type | (Orphanet:1657) |
| Diaphragmatic defect - limb deficiency - skull defect | (Orphanet:2141) |
| Familial multiple nevi flammei | (Orphanet:624) |
| Fanconi anemia | (Orphanet:84) |
| Free sialic acid storage disease | (Orphanet:834) |
| Hypoglossia - hypodactyly | (Orphanet:989) |
| Ichthyosis - oral and digital anomalies | (Orphanet:2272) |
| Intellectual deficit - spasticity - ectrodactyly | (Orphanet:1891) |
| Ito hypomelanosis | (Orphanet:435) |
| Microphthalmia with limb anomalies | (Orphanet:1106) |
| Monomelic amyotrophy | (Orphanet:65684) |
| Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
| Multiple osteochondromas | (Orphanet:321) |
| Nail-patella syndrome | (Orphanet:2614) |
| O'Sullivan-McLeod syndrome | (Orphanet:99965) |
| Phocomelia - ectrodactyly - deafness - sinus arrhythmia | (Orphanet:2878) |
| Ring chromosome 4 | (Orphanet:1447) |
| Roberts syndrome | (Orphanet:3103) |
| Splenogonadal fusion - limb defects - micrognathia | (Orphanet:2063) |
| Thalidomide embryopathy | (Orphanet:3312) |
| Waardenburg syndrome type 3 | (Orphanet:896) |