Abnormality of the upper limb
Symptom Information:
| Symptom ID: | HPO:0002817 | ||||||
| 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) MedDRA: |
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| Database Frequency: | 25 / 7739 | ||||||
| Resource: |
All diseases associated with this symptom:
| Angio-osteohypertrophic syndrome | (Orphanet:2346) |
| Brachydactyly type E | (Orphanet:93387) |
| CLAPO syndrome | (Orphanet:168984) |
| Diaphragmatic defect - limb deficiency - skull defect | (Orphanet:2141) |
| Distal monosomy 17q | (Orphanet:1597) |
| Dysmorphism - short stature - deafness - disorder of sex development | (Orphanet:2282) |
| Focal dermal hypoplasia | (Orphanet:2092) |
| Heart-hand syndrome type 2 | (Orphanet:1350) |
| Heart-hand syndrome type 3 | (Orphanet:1342) |
| Holt-Oram syndrome | (Orphanet:392) |
| Humero-radio-ulnar synostosis | (Orphanet:3266) |
| Klippel-Trénaunay syndrome | (Orphanet:90308) |
| Limb body wall complex | (Orphanet:2369) |
| Localized scleroderma | (Orphanet:90289) |
| Melorheostosis | (Orphanet:2485) |
| Monomelic amyotrophy | (Orphanet:65684) |
| Multiple benign circumferential skin creases on limbs | (Orphanet:2505) |
| O'Sullivan-McLeod syndrome | (Orphanet:99965) |
| PAGOD syndrome | (Orphanet:991) |
| Parkes Weber syndrome | (Orphanet:90307) |
| Proteus syndrome | (Orphanet:744) |
| Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus | (Orphanet:137608) |
| Splenogonadal fusion - limb defects - micrognathia | (Orphanet:2063) |
| Thoraco-abdominal enteric duplication | (Orphanet:1759) |
| X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |