Tapered finger
Symptom Information:
Symptom ID: | HPO:0001182 | ||||||||||||
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) Abnormality of finger(HPO:0001167) Long fingers(HPO:0100807) Tapered finger(HPO:0001182) Abnormality of digit(HPO:0011297) Abnormality of finger(HPO:0001167) Long fingers(HPO:0100807) Tapered finger(HPO:0001182) MedDRA: |
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Database Frequency: | 93 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
16p13.3 microduplication syndrome | (Orphanet:96078) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
2q31.1 microdeletion syndrome | (Orphanet:251014) |
3q29 microdeletion syndrome | (Orphanet:65286) |
6q16 deletion syndrome | (Orphanet:171829) |
8q22.1 microdeletion syndrome | (Orphanet:178303) |
Absence of fingerprints - congenital milia | (Orphanet:1658) |
Acrocallosal syndrome | (Orphanet:36) |
Acrocraniofacial dysostosis | (Orphanet:949) |
Acromegaloid facial appearance syndrome | (Orphanet:965) |
Adult pulmonary Langerhans cell histiocytosis | (Orphanet:99874) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis | (Orphanet:86818) |
Arthrogryposis multiplex congenita | (Orphanet:1037) |
Atkin-Flaitz syndrome | (Orphanet:1193) |
Atypical Rett syndrome | (Orphanet:3095) |
BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME | (OMIM:615722) |
Bohring-Opitz syndrome | (Orphanet:97297) |
Borjeson-Forssman-Lehmann syndrome | (Orphanet:127) |
Bullous dystrophy, macular type | (Orphanet:1867) |
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION | (OMIM:601088) |
CEREBELLOFACIODENTAL SYNDROME | (OMIM:616202) |
CLARK-BARAITSER SYNDROME | (OMIM:300602) |
COLD-INDUCED SWEATING SYNDROME 1 | (OMIM:272430) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Castleman disease | (Orphanet:160) |
Cleft palate - large ears - small head | (Orphanet:2013) |
Cleidocranial dysplasia | (Orphanet:1452) |
Coffin-Lowry syndrome | (Orphanet:192) |
Cohen syndrome | (Orphanet:193) |
Cold-induced sweating syndrome | (Orphanet:157820) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Craniomicromelic syndrome | (Orphanet:1524) |
Craniosynostosis - dysmorphism - brachydactyly | (Orphanet:1535) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 | (OMIM:300672) |
Ehlers-Danlos syndrome, spondylocheirodysplastic type | (Orphanet:157965) |
Eosinophilic granuloma | (Orphanet:99871) |
Erythrokeratodermia variabilis | (Orphanet:317) |
Fine-Lubinsky syndrome | (Orphanet:1272) |
Goldberg-Shprintzen megacolon syndrome | (Orphanet:66629) |
HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION | (OMIM:613870) |
HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS | (OMIM:610680) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 | (OMIM:239300) |
Hereditary sensory and autonomic neuropathy type 2 | (Orphanet:970) |
Hyperphosphatasia-intellectual deficiency syndrome | (Orphanet:247262) |
Ichthyosis - oral and digital anomalies | (Orphanet:2272) |
Intellectual deficit - athetosis - microphthalmia | (Orphanet:1236) |
Intellectual deficit, X-linked - cubitus valgus - dysmorphism | (Orphanet:85280) |
Intellectual deficit, X-linked, Brooks type | (Orphanet:3056) |
Intellectual deficit, X-linked, Pai type | (Orphanet:85322) |
Intellectual deficit, X-linked, Stevenson type | (Orphanet:85325) |
Intellectual deficit, X-linked, Turner type | (Orphanet:85328) |
MEHMO syndrome | (Orphanet:85282) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Micrencephaly - corpus callosum agenesis - abnormal genitalia | (Orphanet:2508) |
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome | (Orphanet:329332) |
Monosomy 9p | (Orphanet:261112) |
Mowat-Wilson syndrome | (Orphanet:2152) |
OTOFACIOCERVICAL SYNDROME 2 | (OMIM:615560) |
Opsismodysplasia | (Orphanet:2746) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
Osteocraniostenosis | (Orphanet:2763) |
PEHO syndrome | (Orphanet:2836) |
POEMS syndrome | (Orphanet:2905) |
PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM | (OMIM:614501) |
Parana hard-skin syndrome | (Orphanet:2812) |
Pierre Robin syndrome - faciodigital anomaly | (Orphanet:2888) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
Qazi-Markouizos syndrome | (Orphanet:3010) |
Ring chromosome 10 | (Orphanet:1438) |
Satoyoshi syndrome | (Orphanet:3130) |
Schilbach-Rott syndrome | (Orphanet:2353) |
Simpson-Golabi-Behmel syndrome type 2 | (Orphanet:79022) |
Split hand - split foot - deafness | (Orphanet:71271) |
Spondyloepimetaphyseal dysplasia - abnormal dentition | (Orphanet:168451) |
Spondylometaphyseal dysplasia, Golden type | (Orphanet:168544) |
Symptomatic form of Coffin-Lowry syndrome in female carriers | (Orphanet:276630) |
Syndromic X-linked intellectual deficit 7 | (Orphanet:85274) |
Syndromic X-linked intellectual deficit due to JARID1C mutation | (Orphanet:85279) |
Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
Toluene embryopathy | (Orphanet:1920) |
Trisomy 17p | (Orphanet:261290) |
Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence | (Orphanet:3201) |
Wiedemann-Steiner syndrome | (Orphanet:319182) |
Wilson-Turner syndrome | (Orphanet:3459) |
X-linked intellectual deficit - hypotonic face | (Orphanet:73220) |
Yunis-Varon syndrome | (Orphanet:3472) |