Broad palm

Symptom Information:

Symptom ID: HPO:0001169
Synonyms:
Broad hand [HPO:0001169]
Wide palm [HPO:0001169]
Large hand [Orphanet:20080]
Broad hands [OMIM:Broad hands]
Large hands (1 patient) [OMIM:Large hands (1 patient)]
Large hands (46%) [OMIM:Large hands (46%)]
Large hands (in patients with PDGFRA mutations) [OMIM:Large hands (in patients with PDGFRA mutations)]
Quality:
Cross references:
HPO:0001176 "Large hands" [Orphanet:20080]
HPO:0001230 "Broad metacarpals" [Orphanet:20080]
Orphanet:20080 "Large hand" [Orphanet:20080]
OMIM: "Broad hands" [OMIM:Broad hands]
OMIM: "Large hands (1 patient)" [OMIM:Large hands (1 patient)]
OMIM: "Large hands (46%)" [OMIM:Large hands (46%)]
OMIM: "Large hands (in patients with PDGFRA mutations)" [OMIM:Large hands (in patients with PDGFRA mutations)]
Is a (Direct Parents):
HPO         Abnormality of the palm
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)
                         Abnormality of the palm(HPO:0100871)
                            Broad palm(HPO:0001169)
MedDRA:
Database Frequency: 43 / 7739
Resource:

All diseases associated with this symptom:

17q11 microdeletion syndrome (Orphanet:97685)
17q11.2 microduplication syndrome (Orphanet:139474)
5p13 microduplication syndrome (Orphanet:329802)
AARSKOG-SCOTT SYNDROME (OMIM:305400)
Acrodysostosis with multiple hormone resistance (Orphanet:280651)
Atkin-Flaitz syndrome (Orphanet:1193)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Bohring-Opitz syndrome (Orphanet:97297)
Brachydactyly type A1 (Orphanet:93388)
CLARK-BARAITSER SYNDROME (OMIM:300602)
Cleft lip/palate - intestinal malrotation - cardiopathy (Orphanet:2001)
Coffin-Lowry syndrome (Orphanet:192)
DYGGVE-MELCHIOR-CLAUSEN DISEASE (OMIM:223800)
Down syndrome (Orphanet:870)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Fountain syndrome (Orphanet:3219)
Gastrointestinal stromal tumor (Orphanet:44890)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Gonadal dysgenesis, XY type - associated anomalies (Orphanet:1770)
Greenberg dysplasia (Orphanet:1426)
Hypertelorism, Teebi type (Orphanet:1519)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 (OMIM:608594)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
Leprechaunism (Orphanet:508)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Osteoglophonic dwarfism (Orphanet:2645)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
Pachygyria - epilepsy - intellectual deficit - dysmorphism (Orphanet:94084)
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism (Orphanet:3085)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Short-rib thoracic dysplasia 2 with or without polydactyly (OMIM:611263)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Simpson-Golabi-Behmel syndrome type 2 (Orphanet:79022)
Smith-Magenis syndrome (Orphanet:819)
Spondyloepimetaphyseal dysplasia, Bieganski type (Orphanet:168448)
Spondyloepimetaphyseal dysplasia, Irapa type (Orphanet:93351)
Spondyloperipheral dysplasia - short ulna (Orphanet:1856)
Tetrasomy 12p (Orphanet:884)
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME (OMIM:300280)
Velo-facial-skeletal syndrome (Orphanet:3424)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)
Weill-Marchesani syndrome (Orphanet:3449)