Adducted thumb
Symptom Information:
Symptom ID: | HPO:0001181 | ||||||
Synonyms: |
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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 digit(HPO:0011297) Abnormality of finger(HPO:0001167) Abnormality of the thumb(HPO:0001172) Adducted thumb(HPO:0001181) Abnormality of the upper limb(HPO:0002817) Abnormality of the hand(HPO:0001155) Abnormality of finger(HPO:0001167) Abnormality of the thumb(HPO:0001172) Adducted thumb(HPO:0001181) MedDRA: |
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Database Frequency: | 31 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
3-phosphoglycerate dehydrogenase deficiency | (Orphanet:79351) |
ALDH18A1-related De Barsy syndrome | (Orphanet:35664) |
ALG3-CDG | (Orphanet:79321) |
Autosomal recessive cutis laxa type 2B | (Orphanet:357064) |
CEREBROOCULOFACIOSKELETAL SYNDROME 4 | (OMIM:610758) |
COLD-INDUCED SWEATING SYNDROME 1 | (OMIM:272430) |
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTALDELAY | (OMIM:616266) |
Christianson syndrome | (Orphanet:85278) |
Cold-induced sweating syndrome | (Orphanet:157820) |
Congenital contractural arachnodactyly | (Orphanet:115) |
De Barsy syndrome | (Orphanet:2962) |
Digitotalar dysmorphism | (Orphanet:1146) |
Distal arthrogryposis type 5D | (Orphanet:329457) |
Dyssegmental dysplasia, Rolland-Desbuquois type | (Orphanet:156731) |
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 2 | (OMIM:615539) |
Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
Hydrocephalus with stenosis of aqueduct of Sylvius | (Orphanet:2182) |
Hypertryptophanemia | (Orphanet:2224) |
Isolated sedoheptulokinase deficiency | (ORPHA:440713) |
L1 syndrome | (Orphanet:275543) |
MASA syndrome | (Orphanet:2466) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 7 | (OMIM:614643) |
RFT1-CDG | (Orphanet:244310) |
SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE | (OMIM:612936) |
Severe intellectual deficit and progressive spastic paraplegia | (Orphanet:280763) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
Syndactyly - camptodactyly and clinodactyly of fifth fingers - bifid toes | (Orphanet:357332) |
TEMPLE-BARAITSER SYNDROME | (OMIM:611816) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
X-linked complicated spastic paraplegia type 1 | (Orphanet:306617) |