Large hands

Symptom Information:

Symptom ID: HPO:0001176
Synonyms:
Disproportionately large hands [HPO:0001176]
Broad palm [Orphanet:20080]
Disproportionately large hands [OMIM:Disproportionately large hands]
Large hands [OMIM:Large hands]
Large hand [Orphanet:20080]
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:0001169 "Broad palm" [Orphanet:20080]
HPO:0001230 "Broad metacarpals" [Orphanet:20080]
Orphanet:20080 "Large hand" [Orphanet:20080]
OMIM: "Disproportionately large hands" [OMIM:Disproportionately large hands]
OMIM: "Large hands" [OMIM:Large 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         Abnormal hand morphology
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)
                         Abnormal hand morphology(HPO:0005922)
                            Large hands(HPO:0001176)
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)
ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA (OMIM:102100)
ASPARAGINE SYNTHETASE DEFICIENCY (OMIM:615574)
Acromegaloid facial appearance syndrome (Orphanet:965)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
CHROMOSOME Xq26.3 DUPLICATION SYNDROME (OMIM:300942)
COCKAYNE SYNDROME, TYPE III (OMIM:216411)
Cockayne syndrome (Orphanet:191)
Coffin-Lowry syndrome (Orphanet:192)
Congenital hypothyroidism due to developmental anomaly (Orphanet:95711)
DERMATOLEUKODYSTROPHY (OMIM:221790)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
Diencephalic syndrome (Orphanet:1672)
Distal trisomy 18q (Orphanet:1716)
Fountain syndrome (Orphanet:3219)
Gastrointestinal stromal tumor (Orphanet:44890)
Gonadal dysgenesis, XY type - associated anomalies (Orphanet:1770)
Intellectual deficit, Wolff type (Orphanet:3080)
Intellectual deficit, X-linked, Siderius type (Orphanet:85287)
Intellectual deficit, X-linked, Stevenson type (Orphanet:85325)
Kyphomelic dysplasia (Orphanet:1801)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 (OMIM:608594)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
Leprechaunism (Orphanet:508)
MOMO syndrome (Orphanet:2563)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Monosomy 22q13 (Orphanet:48652)
Neu-Laxova syndrome (Orphanet:2671)
Neuroectodermal-endocrine syndrome (Orphanet:2676)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
SOTOS SYNDROME 1 (OMIM:117550)
Sotos syndrome (Orphanet:821)
Symptomatic form of Coffin-Lowry syndrome in female carriers (Orphanet:276630)
Syndromic X-linked intellectual deficit due to JARID1C mutation (Orphanet:85279)
Tetrasomy 18p (Orphanet:3307)
Trisomy 12p (Orphanet:1699)
Velo-facial-skeletal syndrome (Orphanet:3424)
Weaver syndrome (Orphanet:3447)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Zunich-Kaye syndrome (Orphanet:3474)