Small hand
Symptom Information:
Symptom ID: | HPO:0200055 | ||||||||||||
Synonyms: |
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Quality: | |||||||||||||
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) 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) 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) Abnormality of the hand(HPO:0001155) Aplasia/hypoplasia involving bones of the hand(HPO:0005927) Small hand(HPO:0200055) Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496) Aplasia/hypoplasia involving bones of the hand(HPO:0005927) Small hand(HPO:0200055) MedDRA: |
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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) |