Long palm

Symptom Information:

Symptom ID: HPO:0011302
Long hand/arachnodactyly [Orphanet:20120]
Cross references:
Orphanet:20120 "Long hand/arachnodactyly" [Orphanet:20120]
Is a (Direct Parents):
HPO         Abnormality of the palm
Orphanet Abnormality of the hand
Orphanet Arachnodactyly
Is a (Whole tree): HPO:
    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)
Database Frequency: 70 / 7739

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)