Large hands
Symptom Information:
Symptom ID: | HPO:0001176 | ||||||||
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) 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: |
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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) |