Ulnar deviation of the hand or of fingers of the hand

Symptom Information:

Symptom ID: HPO:0001193
Synonyms:
Ulnar deviation of hands [HPO:0001193]
Ulnar deviation of the hands [HPO:0001193]
Ulnar deviation of hands [OMIM:Ulnar deviation of hands]
Ulnar deviation of the hands [OMIM:Ulnar deviation of the hands]
Quality:
Cross references:
OMIM: "Ulnar deviation of hands" [OMIM:Ulnar deviation of hands]
OMIM: "Ulnar deviation of the hands" [OMIM:Ulnar deviation of the hands]
Is a (Direct Parents):
HPO         Deviation of the hand or of fingers 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)
                            Ulnar deviation of the hand or of fingers of the hand(HPO:0001193)
MedDRA:
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

ANE syndrome (Orphanet:157954)
Craniofacial-deafness-hand syndrome (Orphanet:1529)
Digitotalar dysmorphism (Orphanet:1146)
Endocrine-cerebro-osteodysplasia syndrome (Orphanet:199332)
FETAL AKINESIA DEFORMATION SEQUENCE (OMIM:208150)
Fetal akinesia deformation sequence (Orphanet:994)
Freeman-Sheldon syndrome (Orphanet:2053)
Goodman syndrome (Orphanet:65798)
Gordon syndrome (Orphanet:376)
Mesomelia-synostoses syndrome (Orphanet:2496)
Multicentric carpo-tarsal osteolysis with or without nephropathy (Orphanet:2774)
OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE (OMIM:258650)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL (OMIM:602613)
Sheldon-Hall syndrome (Orphanet:1147)
Upper limb mesomelic dysplasia (Orphanet:2497)
Zellweger syndrome (Orphanet:912)