Finger symphalangism
Symptom Information:
Symptom ID: | HPO:0009700 | ||||||||||||||||||||||||||||||||||||||||||
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 upper limb(HPO:0002817) Abnormality of the hand(HPO:0001155) Synostosis involving bones of the hand(HPO:0004278) Finger symphalangism(HPO:0009700) Abnormality of upper limb joint(HPO:0009810) Synostosis involving bones of the upper limbs(HPO:0100238) Synostosis involving bones of the hand(HPO:0004278) Finger symphalangism(HPO:0009700) Abnormal joint morphology(HPO:0001367) Abnormality of upper limb joint(HPO:0009810) Synostosis involving bones of the upper limbs(HPO:0100238) Synostosis involving bones of the hand(HPO:0004278) Finger symphalangism(HPO:0009700) Abnormality of joint mobility(HPO:0011729) Synostosis of joints(HPO:0100240) Synostosis involving bones of the upper limbs(HPO:0100238) Synostosis involving bones of the hand(HPO:0004278) Finger symphalangism(HPO:0009700) Synostosis involving digits(HPO:0100262) Finger symphalangism(HPO:0009700) 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) Finger symphalangism(HPO:0009700) |
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Database Frequency: | 55 / 7739 | ||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Aphalangy - syndactyly - microcephaly | (Orphanet:1113) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Brachydactyly type A1 | (Orphanet:93388) |
Brachydactyly type A2 | (Orphanet:93396) |
Brachydactyly type A4 | (Orphanet:93394) |
Brachydactyly type B | (Orphanet:93383) |
Brachydactyly type B2 | (Orphanet:140908) |
Brachydactyly type C | (Orphanet:93384) |
Brachydactyly-syndactyly, Zhao type | (Orphanet:93409) |
Brachymorphism - onychodysplasia - dysphalangism | (Orphanet:1292) |
CORNELIA DE LANGE SYNDROME 4 | (OMIM:614701) |
CREE MENTAL RETARDATION SYNDROME | (OMIM:606851) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Caudal appendage - deafness | (Orphanet:1123) |
Char syndrome | (Orphanet:46627) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Craniosynostosis and dental anomalies | (Orphanet:284149) |
Curry-Jones syndrome | (Orphanet:1553) |
Deafness - onychodystrophy | (Orphanet:3231) |
Diastrophic dwarfism | (Orphanet:628) |
Distal monosomy 7q36 | (Orphanet:1636) |
Distal symphalangism | (Orphanet:3248) |
Ectrodactyly - polydactyly | (Orphanet:1892) |
Faciocardiorenal syndrome | (Orphanet:1973) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fuhrmann syndrome | (Orphanet:2854) |
Greig cephalopolysyndactyly syndrome | (Orphanet:380) |
Hypertelorism - hypospadias - polysyndactyly syndrome | (Orphanet:2211) |
Jackson-Weiss syndrome | (Orphanet:1540) |
Joubert syndrome 17 | (OMIM:614615) |
Joubert syndrome 20 | (OMIM:614970) |
Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
MULTIPLE SYNOSTOSES SYNDROME 2 | (OMIM:610017) |
Mesoaxial synostotic syndactyly with phalangeal reduction | (Orphanet:157801) |
Microphthalmia - microtia - fetal akinesia | (Orphanet:2547) |
Mononen-Karnes-Senac syndrome | (Orphanet:2565) |
Multiple synostoses syndrome | (Orphanet:3237) |
Oliver syndrome | (Orphanet:2920) |
Ophthalmomandibulomelic dysplasia | (Orphanet:2741) |
Pelviscapular dysplasia | (Orphanet:93333) |
Pfeiffer syndrome | (Orphanet:710) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Proximal symphalangism | (Orphanet:3250) |
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) |
Syndactyly type 1 | (Orphanet:93402) |
Syndactyly type 2 | (Orphanet:93403) |
Syndrome with brachydactyly | (Orphanet:69028) |
Synpolydactyly type 2 | (Orphanet:295197) |
Timothy syndrome | (Orphanet:65283) |
Trismus - pseudocamptodactyly | (Orphanet:3377) |
Ulnar/fibula ray defect - brachydactyly | (Orphanet:52056) |