Ulnar deviation of the hand or of fingers of the hand
Symptom Information:
Symptom ID: | HPO:0001193 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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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) 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: |
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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) |