Broad palm
Symptom Information:
Symptom ID: | HPO:0001169 | |||||||
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) Abnormality of the palm(HPO:0100871) Broad palm(HPO:0001169) 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) |
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) |