Arachnodactyly
Symptom Information:
Symptom ID: | HPO:0001166 | ||||||||||||
Synonyms: |
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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 lower limb(HPO:0002814) Abnormality of the foot(HPO:0001760) Abnormality of toe(HPO:0001780) Long toe(HPO:0010511) 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) 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) 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) |
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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) |