Long palm
Symptom Information:
Symptom ID: | HPO:0011302 | ||||||
Synonyms: |
|
||||||
Quality: | |||||||
Cross references: |
|
||||||
Is a (Direct Parents): |
|
||||||
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) Long palm(HPO:0011302) MedDRA: |
||||||
Database Frequency: | 70 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
10q22.3q23.3 microdeletion syndrome | (Orphanet:276413) |
15q24 microdeletion syndrome | (Orphanet:94065) |
16p13.11 microduplication syndrome | (Orphanet:261243) |
17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |
2q32q33 microdeletion syndrome | (Orphanet:251019) |
46,XX gonadal dysgenesis | (Orphanet:243) |
Antley-Bixler syndrome | (Orphanet:83) |
Arachnodactyly - abnormal ossification - intellectual deficit | (Orphanet:1129) |
Arachnodactyly - intellectual deficit - dysmorphism | (Orphanet:1130) |
Arterial tortuosity syndrome | (Orphanet:3342) |
Arthrogryposis-like hand anomaly - sensorineural deafness | (Orphanet:1144) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
Camptodactyly - fibrous tissue hyperplasia - skeletal dysplasia | (Orphanet:1321) |
Classical homocystinuria | (Orphanet:394) |
Cohen syndrome | (Orphanet:193) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Cryptorchidism - arachnodactyly - intellectual deficit | (Orphanet:1548) |
Cutis laxa-Marfanoid syndrome | (Orphanet:171719) |
Distal 22q11.2 microdeletion syndrome | (Orphanet:261330) |
Distal monosomy 19p13.3 | (Orphanet:96129) |
Distal trisomy 15q | (Orphanet:1707) |
Distal trisomy 18q | (Orphanet:1716) |
Ectodermal dysplasia - sensorineural deafness | (Orphanet:1883) |
Edinburgh malformation syndrome | (Orphanet:1895) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria | (Orphanet:1035) |
Eye defects - arachnodactyly - cardiopathy | (Orphanet:2725) |
Familial visceral myopathy | (Orphanet:2604) |
Frontometaphyseal dysplasia | (Orphanet:1826) |
Fryns-Smeets-Thiry syndrome | (Orphanet:2058) |
Gorlin syndrome | (Orphanet:377) |
Haim-Munk syndrome | (Orphanet:2342) |
Harrod syndrome | (Orphanet:2115) |
Hydrocephaly - tall stature - joint laxity | (Orphanet:2181) |
Imperforate oropharynx - costo vetebral anomalies | (Orphanet:2759) |
Intellectual deficit, X-linked - seizures - psoriasis | (Orphanet:3052) |
Intellectual deficit, X-linked, Armfield type | (Orphanet:85276) |
Intellectual deficit, X-linked, Snyder type | (Orphanet:3063) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Kousseff syndrome | (Orphanet:2351) |
Loeys-Dietz syndrome type 1 | (Orphanet:60030) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Marden-Walker syndrome | (Orphanet:2461) |
Marfan syndrome | (Orphanet:558) |
Marfanoid habitus - intellectual deficit, autosomal recessive | (Orphanet:2463) |
Microcephaly - glomerulonephritis - marfanoid habitus | (Orphanet:2172) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Non-distal trisomy 13q | (Orphanet:1702) |
Oculocerebral hypopigmentation syndrome, Cross type | (Orphanet:2719) |
Oculocerebral hypopigmentation syndrome, Preus type | (Orphanet:2720) |
Oculocerebrofacial syndrome, Kaufman type | (Orphanet:2707) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Papillon-Lefèvre syndrome | (Orphanet:678) |
Paraplegia - intellectual deficit - hyperkeratosis | (Orphanet:2824) |
Prolidase deficiency | (Orphanet:742) |
Schilbach-Rott syndrome | (Orphanet:2353) |
Short stature - craniofacial anomalies - genital hypoplasia | (Orphanet:2994) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
Stickler syndrome | (Orphanet:828) |
Trisomy 1q | (Orphanet:261344) |
Van den Ende-Gupta syndrome | (Orphanet:2460) |
Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay | (Orphanet:73246) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
X-linked intellectual deficit with marfanoid habitus | (Orphanet:776) |
Zellweger-like syndrome without peroxisomal anomalies | (Orphanet:50812) |