Arachnodactyly

Symptom Information:

Symptom ID: HPO:0001166
Synonyms:
Long slender fingers [HPO:0001166]
Long, slender fingers [HPO:0001166]
Long fingers [Orphanet:20120]
Arachnodactyly [OMIM:Arachnodactyly]
Long slender fingers [OMIM:Long slender fingers]
Long, slender fingers [OMIM:Long, slender fingers]
Long hand/arachnodactyly [Orphanet:20120]
Arachnodactyly (in some patients) [OMIM:Arachnodactyly (in some patients)]
Long fingers (2 patient) [OMIM:Long fingers (2 patient)]
Long fingers (rare) [OMIM:Long fingers (rare)]
Long, slender fingers (61%) [OMIM:Long, slender fingers (61%)]
Arachnodactyly [MedDRA:10063847]
Quality:
Cross references:
HPO:0100807 "Long fingers" [Orphanet:20120]
Orphanet:20120 "Long hand/arachnodactyly" [Orphanet:20120]
OMIM: "Arachnodactyly" [OMIM:Arachnodactyly]
OMIM: "Long slender fingers" [OMIM:Long slender fingers]
OMIM: "Long, slender fingers" [OMIM:Long, slender fingers]
OMIM: "Arachnodactyly (in some patients)" [OMIM:Arachnodactyly (in some patients)]
OMIM: "Long fingers (2 patient)" [OMIM:Long fingers (2 patient)]
OMIM: "Long fingers (rare)" [OMIM:Long fingers (rare)]
OMIM: "Long, slender fingers (61%)" [OMIM:Long, slender fingers (61%)]
Is a (Direct Parents):
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
HPO         Long toe
Orphanet Abnormality of the hand
HPO         Long fingers
HPO         Slender finger
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 lower limb(HPO:0002814)
                      Abnormality of the foot(HPO:0001760)
                         Abnormality of toe(HPO:0001780)
                            Long toe(HPO:0010511)
                               Arachnodactyly(HPO:0001166)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of finger(HPO:0001167)
                            Slender finger(HPO:0001238)
                               Arachnodactyly(HPO:0001166)
                            Long fingers(HPO:0100807)
                               Arachnodactyly(HPO:0001166)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Slender finger(HPO:0001238)
                            Arachnodactyly(HPO:0001166)
                         Long fingers(HPO:0100807)
                            Arachnodactyly(HPO:0001166)
                      Abnormality of toe(HPO:0001780)
                         Long toe(HPO:0010511)
                            Arachnodactyly(HPO:0001166)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396)
       Musculoskeletal and connective tissue disorders of limbs congenital(MedDRA:10028381)
          Arachnodactyly(HPO:0001166)
Database Frequency: 62 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
17q12 microdeletion syndrome (Orphanet:261265)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q32q33 microdeletion syndrome (Orphanet:251019)
5p13 microduplication syndrome (Orphanet:329802)
ACHARD SYNDROME (OMIM:100700)
ALPHA-2-DEFICIENT COLLAGEN DISEASE (OMIM:203760)
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
AORTIC ANEURYSM, FAMILIAL THORACIC 9 (OMIM:616166)
Aneurysm - osteoarthritis syndrome (Orphanet:284984)
Antley-Bixler syndrome (Orphanet:83)
Arterial tortuosity syndrome (Orphanet:3342)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Autosomal recessive cutis laxa type 1 (Orphanet:90349)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA (OMIM:211930)
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB (OMIM:614437)
Camptodactyly - tall stature - scoliosis - hearing loss (Orphanet:85164)
Classical homocystinuria (Orphanet:394)
Congenital contractural arachnodactyly (Orphanet:115)
Congenital lethal myopathy, Compton-North type (Orphanet:210163)
Cutis laxa-Marfanoid syndrome (Orphanet:171719)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 (OMIM:601776)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 2 (OMIM:615539)
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 (OMIM:130070)
EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE (OMIM:615923)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Ehlers-Danlos syndrome, musculocontractural type (Orphanet:2953)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Frontometaphyseal dysplasia (Orphanet:1826)
Haim-Munk syndrome (Orphanet:2342)
Harrod syndrome (Orphanet:2115)
Intellectual deficit, X-linked, Raymond type (Orphanet:163953)
Koolen-De Vries syndrome (Orphanet:96169)
LOEYS-DIETZ SYNDROME 1 (OMIM:609192)
LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
LOEYS-DIETZ SYNDROME 4 (OMIM:614816)
LUJAN-FRYNS SYNDROME (OMIM:309520)
Lethal occipital encephalocele-skeletal dysplasia syndrome (Orphanet:293925)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
MARFANOID HABITUS WITH SITUS INVERSUS (OMIM:609008)
MARFANOID HYPERMOBILITY SYNDROME (OMIM:154750)
Marden-Walker syndrome (Orphanet:2461)
Marfan syndrome type 1 (Orphanet:284963)
Marfanoid habitus - intellectual deficit, autosomal recessive (Orphanet:2463)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Microcephaly - glomerulonephritis - marfanoid habitus (Orphanet:2172)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
OSTEOGENESIS IMPERFECTA, TYPE XIII (OMIM:614856)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES (OMIM:602249)
Pseudoaminopterin syndrome (Orphanet:221120)
RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION (OMIM:268050)
RIENHOFF SYNDROME (OMIM:615582)
STICKLER SYNDROME, TYPE I (OMIM:108300)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Stickler syndrome (Orphanet:828)
Stickler syndrome type 2 (Orphanet:90654)
Van den Ende-Gupta syndrome (Orphanet:2460)
X-linked centronuclear myopathy (Orphanet:596)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome (Orphanet:85295)