Cutaneous syndactyly of toes
Symptom Information:
Symptom ID: | HPO:0010621 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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) Toe syndactyly(HPO:0001770) Cutaneous syndactyly of toes(HPO:0010621) Abnormality of digit(HPO:0011297) Syndactyly(HPO:0001159) Toe syndactyly(HPO:0001770) Cutaneous syndactyly of toes(HPO:0010621) Abnormality of toe(HPO:0001780) Toe syndactyly(HPO:0001770) Cutaneous syndactyly of toes(HPO:0010621) 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) Cutaneous syndactyly of toes(HPO:0010621) |
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Database Frequency: | 36 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Absence of fingerprints - congenital milia | (Orphanet:1658) |
Blepharophimosis - ptosis - esotropia - syndactyly - short stature | (Orphanet:2057) |
Brachydactyly type A2 | (Orphanet:93396) |
Brachydactyly type B | (Orphanet:93383) |
Brachydactyly type B2 | (Orphanet:140908) |
CORNELIA DE LANGE SYNDROME 4 | (OMIM:614701) |
CREE MENTAL RETARDATION SYNDROME | (OMIM:606851) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cranioectodermal dysplasia 4 | (OMIM:614378) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Craniosynostosis and dental anomalies | (Orphanet:284149) |
Curry-Jones syndrome | (Orphanet:1553) |
Deafness - onychodystrophy, autosomal dominant | (Orphanet:79499) |
Faciocardiorenal syndrome | (Orphanet:1973) |
Focal dermal hypoplasia | (Orphanet:2092) |
Greig cephalopolysyndactyly syndrome | (Orphanet:380) |
Hennekam syndrome | (Orphanet:2136) |
Hypertelorism - hypospadias - polysyndactyly syndrome | (Orphanet:2211) |
Joubert syndrome 17 | (OMIM:614615) |
Joubert syndrome 20 | (OMIM:614970) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
MULTIPLE SYNOSTOSES SYNDROME 1 | (OMIM:186500) |
POLYDACTYLY, POSTAXIAL, TYPE A5 | (OMIM:263450) |
Pelviscapular dysplasia | (Orphanet:93333) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Rosselli-Gulienetti syndrome | (Orphanet:90339) |
SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIB | (OMIM:615087) |
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY | (OMIM:614800) |
Saethre-Chotzen syndrome | (Orphanet:794) |
Symphalangism with multiple anomalies of hands and feet | (Orphanet:3246) |
Synpolydactyly type 2 | (Orphanet:295197) |
Timothy syndrome | (Orphanet:65283) |
Trismus - pseudocamptodactyly | (Orphanet:3377) |
Ulnar/fibula ray defect - brachydactyly | (Orphanet:52056) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |