Adducted thumb

Symptom Information:

Symptom ID: HPO:0001181
Synonyms:
Adducted thumbs [HPO:0001181]
Adducted thumb [OMIM:Adducted thumb]
Adducted thumbs [OMIM:Adducted thumbs]
Clasp thumb/thumb adduction/distal thumb phalangeal bone deviated/large [Orphanet:20780]
Clasped thumb [Orphanet:20780]
Clasped thumb [OMIM:Clasped thumb]
Quality:
Cross references:
HPO:0001234 "Hitchhiker thumb" [Orphanet:20780]
Orphanet:20780 "Clasp thumb/thumb adduction/distal thumb phalangeal bone deviated/large" [Orphanet:20780]
OMIM: "Adducted thumb" [OMIM:Adducted thumb]
OMIM: "Adducted thumbs" [OMIM:Adducted thumbs]
OMIM: "Clasped thumb" [OMIM:Clasped thumb]
Is a (Direct Parents):
Orphanet Thumb anomalies (excluding hypoplasia)
HPO         Abnormality of the thumb
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)
                         Abnormality of finger(HPO:0001167)
                            Abnormality of the thumb(HPO:0001172)
                               Adducted thumb(HPO:0001181)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Abnormality of the thumb(HPO:0001172)
                            Adducted thumb(HPO:0001181)
MedDRA:
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)