Radial deviation of the hand

Symptom Information:

Symptom ID: HPO:0009486
Synonyms:
Radial deviation of hands [HPO:0009486]
Radial Deviation of hand [Orphanet:20040]
Radial deviation of hand [HPO:0009486]
Radial deviation of hand (finding) [Orphanet:20040]
Radial deviation of hand [Orphanet:20040]
Radial deviation of hands [OMIM:Radial deviation of hands]
Radial club hand [Orphanet:20040]
Quality:
Cross references:
HPO:0009485 "Radial deviation of the hand or of fingers of the hand" [Orphanet:20040]
Orphanet:20040 "Radial club hand" [Orphanet:20040]
OMIM: "Radial deviation of hands" [OMIM:Radial deviation of hands]
UMLS:C0575803 "Radial deviation of hand" [Orphanet:20040]
Is a (Direct Parents):
HPO         Radial deviation of the hand or of fingers of the hand
Orphanet Abnormality of the hand
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)
                         Deviation of the hand or of fingers of the hand(HPO:0009484)
                            Radial deviation of the hand or of fingers of the hand(HPO:0009485)
                               Radial deviation of the hand(HPO:0009486)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Acro-renal-ocular syndrome (Orphanet:959)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Brachydactyly - preaxial hallux varus (Orphanet:1278)
Holoprosencephaly - caudal dysgenesis (Orphanet:2165)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Lethal faciocardiomelic dysplasia (Orphanet:1972)
Okihiro syndrome (Orphanet:93293)
Phocomelia - ectrodactyly - deafness - sinus arrhythmia (Orphanet:2878)
Richieri Costa-Pereira syndrome (Orphanet:3102)
Tetraploidy (Orphanet:3305)
Thalidomide embryopathy (Orphanet:3312)
Trisomy 4p (Orphanet:1738)
X-linked spondyloepimetaphyseal dysplasia (Orphanet:93349)