Abnormality of the upper limb

Symptom Information:

Symptom ID: HPO:0002817
Cross references:
Is a (Direct Parents):
HPO         Abnormal arm span
HPO         Abnormality of upper limb bone
HPO         Abnormality of limb bone morphology
Is a (Whole tree): HPO:
    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)
Database Frequency: 25 / 7739

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)