Small hand

Symptom Information:

Symptom ID: HPO:0200055
Synonyms:
Disproportionately small hands [HPO:0200055]
SMALL HANDS [HPO:0200055]
Small hands [OMIM:Small hands]
Small hands (62%) [OMIM:Small hands (62%)]
Small hands (84%) [OMIM:Small hands (84%)]
Small hands (<25th percentile for height age) [OMIM:Small hands (<25th percentile for height age)]
Small hands (deletion patients) [OMIM:Small hands (deletion patients)]
Small hands (in some patients) [OMIM:Small hands (in some patients)]
Small hands (male and female) [OMIM:Small hands (male and female)]
Small hand/acromicria [Orphanet:20100]
Small hand [Orphanet:20100]
Small hand (finding) [Orphanet:20100]
Quality:
Cross references:
Orphanet:20100 "Small hand/acromicria" [Orphanet:20100]
OMIM: "Small hands" [OMIM:Small hands]
OMIM: "Small hands (62%)" [OMIM:Small hands (62%)]
OMIM: "Small hands (84%)" [OMIM:Small hands (84%)]
OMIM: "Small hands (<25th percentile for height age)" [OMIM:Small hands (<25th percentile for height age)]
OMIM: "Small hands (deletion patients)" [OMIM:Small hands (deletion patients)]
OMIM: "Small hands (in some patients)" [OMIM:Small hands (in some patients)]
OMIM: "Small hands (male and female)" [OMIM:Small hands (male and female)]
UMLS:C0575802 "Small hand" [Orphanet:20100]
Is a (Direct Parents):
HPO         Aplasia/hypoplasia involving bones of the hand
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)
                   Aplasia/hypoplasia of the extremities(HPO:0009815)
                      Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                         Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                            Small hand(HPO:0200055)
                   Abnormality of the upper limb(HPO:0002817)
                      Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                         Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                            Small hand(HPO:0200055)
                      Abnormality of the hand(HPO:0001155)
                         Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                            Small hand(HPO:0200055)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia of the extremities(HPO:0009815)
                   Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                      Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                         Small hand(HPO:0200055)
MedDRA:
Database Frequency: 71 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
2q23.1 microdeletion syndrome (Orphanet:228402)
2q37 microdeletion syndrome (Orphanet:1001)
4q21 microdeletion syndrome (Orphanet:238750)
Aarskog-Scott syndrome (Orphanet:915)
Acrofacial dysostosis, Catania type (Orphanet:1786)
Acrofacial dysostosis, Palagonia type (Orphanet:1787)
Acrofacial dysostosis, Weyers type (Orphanet:952)
Acrogeria (Orphanet:2500)
Acromicric dysplasia (Orphanet:969)
Aicardi syndrome (Orphanet:50)
Atypical Rett syndrome (Orphanet:3095)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant nonsyndromic intellectual deficit (Orphanet:178469)
Autosomal recessive Kenny-Caffey syndrome (Orphanet:93324)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Brachydactyly-long thumb syndrome (Orphanet:2946)
Böök syndrome (Orphanet:1262)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2 (OMIM:610185)
CONGENITAL DISORDER OF DEGLYCOSYLATION (OMIM:615273)
CORNELIA DE LANGE SYNDROME 2 (OMIM:300590)
CORNELIA DE LANGE SYNDROME 3 (OMIM:610759)
CORNELIA DE LANGE SYNDROME 5 (OMIM:300882)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cartilage-hair hypoplasia (Orphanet:175)
Cornelia de Lange syndrome (Orphanet:199)
DPM1-CDG (Orphanet:79322)
Desbuquois syndrome (Orphanet:1425)
Distal monosomy 17q (Orphanet:1597)
Dubowitz syndrome (Orphanet:235)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 (OMIM:300672)
Ear-patella-short stature syndrome (Orphanet:2554)
FIBROCHONDROGENESIS 1 (OMIM:228520)
Fibrochondrogenesis (Orphanet:2021)
GMS syndrome (Orphanet:2090)
Goldberg-Shprintzen megacolon syndrome (Orphanet:66629)
Grubben-de Cock-Borghgraef syndrome (Orphanet:2101)
HELSMOORTEL-VAN DER AA SYNDROME (OMIM:615873)
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES (OMIM:614684)
Hallermann-Streiff syndrome (Orphanet:2108)
Hennekam syndrome (Orphanet:2136)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
Intellectual deficit, X-linked, Armfield type (Orphanet:85276)
Intellectual deficit, X-linked, Vitale type (Orphanet:85289)
Kabuki syndrome (Orphanet:2322)
MEIER-GORLIN SYNDROME 1 (OMIM:224690)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 (OMIM:614563)
MENTAL RETARDATION, X-LINKED 91 (OMIM:300577)
MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE (OMIM:616051)
Microcephalic osteodysplastic dysplasia, Saul-Wilson type (Orphanet:85172)
Monosomy 5p (Orphanet:281)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
Multiple epiphyseal dysplasia (Orphanet:251)
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:257850)
Pachydermoperiostosis (Orphanet:2796)
Pentasomy X (Orphanet:11)
Prader-Willi syndrome (Orphanet:739)
Rothmund-Thomson syndrome (Orphanet:2909)
Ruvalcaba syndrome (Orphanet:3121)
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY (OMIM:181405)
SCHAAF-YANG SYNDROME (OMIM:615547)
Sanjad-Sakati syndrome (Orphanet:2323)
Schinzel-Giedion syndrome (Orphanet:798)
Short stature - valvular heart disease - characteristic facies (Orphanet:2868)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Subaortic stenosis - short stature (Orphanet:3191)
TEMPLE SYNDROME (OMIM:616222)
Werner syndrome (Orphanet:902)
Wilson-Turner syndrome (Orphanet:3459)
Xq27.3q28 duplication syndrome (Orphanet:261483)