2-3 toe syndactyly
Symptom Information:
Symptom ID: | HPO:0004691 | ||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||||||||||
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) 2-3 toe syndactyly(HPO:0004691) Abnormality of digit(HPO:0011297) Abnormality of toe(HPO:0001780) Toe syndactyly(HPO:0001770) 2-3 toe syndactyly(HPO:0004691) Syndactyly(HPO:0001159) Toe syndactyly(HPO:0001770) 2-3 toe syndactyly(HPO:0004691) MedDRA: |
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Database Frequency: | 50 / 7739 | ||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ADAMS-OLIVER SYNDROME 3 | (OMIM:614814) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 16 | (OMIM:615993) |
Brachydactyly type A2 | (Orphanet:93396) |
CARDIAC MALFORMATION, CLEFT LIP/PALATE, MICROCEPHALY AND DIGITAL ANOMALIES | (OMIM:600987) |
COLD-INDUCED SWEATING SYNDROME 2 | (OMIM:610313) |
CORNELIA DE LANGE SYNDROME 4 | (OMIM:614701) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Choanal atresia - deafness - cardiac defects - dysmorphism | (Orphanet:1200) |
Cornelia de Lange syndrome | (Orphanet:199) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Craniosynostosis and dental anomalies | (Orphanet:284149) |
Craniosynostosis, Philadelphia type | (Orphanet:1527) |
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY | (OMIM:600906) |
Eyebrow duplication - syndactyly | (Orphanet:3172) |
Faciocardiorenal syndrome | (Orphanet:1973) |
Feingold syndrome | (Orphanet:1305) |
Focal dermal hypoplasia | (Orphanet:2092) |
Greig cephalopolysyndactyly syndrome | (Orphanet:380) |
HUNTER-MACDONALD SYNDROME | (OMIM:611962) |
HYDRANENCEPHALY WITH RENAL APLASIA-DYSPLASIA | (OMIM:236500) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Hypertelorism - hypospadias - polysyndactyly syndrome | (Orphanet:2211) |
Hypertelorism-microtia-facial clefting syndrome | (Orphanet:2213) |
Jackson-Weiss syndrome | (Orphanet:1540) |
Joubert syndrome 17 | (OMIM:614615) |
Joubert syndrome 20 | (OMIM:614970) |
MULTIPLE SYNOSTOSES SYNDROME 1 | (OMIM:186500) |
Monosomy 22q13 | (Orphanet:48652) |
Mulibrey nanism | (Orphanet:2576) |
Multiple synostoses syndrome | (Orphanet:3237) |
Myhre syndrome | (Orphanet:2588) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Pelviscapular dysplasia | (Orphanet:93333) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY | (OMIM:614800) |
Saethre-Chotzen syndrome | (Orphanet:794) |
Scalp-ear-nipple syndrome | (Orphanet:2036) |
Sialuria | (Orphanet:3166) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Symphalangism with multiple anomalies of hands and feet | (Orphanet:3246) |
Syndactyly type 4 | (Orphanet:93405) |
Synpolydactyly type 2 | (Orphanet:295197) |
Timothy syndrome | (Orphanet:65283) |
Townes-Brocks syndrome | (Orphanet:857) |
Ulnar/fibula ray defect - brachydactyly | (Orphanet:52056) |
Warsaw breakage syndrome | (Orphanet:280558) |