Tapered finger

Symptom Information:

Symptom ID: HPO:0001182
Synonyms:
Distally tapering fingers [HPO:0001182]
TAPERED FINGERS [HPO:0001182]
Tapered fingertips [HPO:0001182]
Tapering fingers [HPO:0001182]
Tapering fingers (finding) [Orphanet:20360]
Distally tapering fingers [OMIM:Distally tapering fingers]
Tapered fingers [OMIM:Tapered fingers]
Tapered fingertips [OMIM:Tapered fingertips]
Tapering fingers [OMIM:Tapering fingers]
Tapered fingers [Orphanet:20360]
Tapered fingers (in some patients) [OMIM:Tapered fingers (in some patients)]
Tapering fingers (in some patients) [OMIM:Tapering fingers (in some patients)]
Quality:
Cross references:
Orphanet:20360 "Tapered fingers" [Orphanet:20360]
OMIM: "Distally tapering fingers" [OMIM:Distally tapering fingers]
OMIM: "Tapered fingers" [OMIM:Tapered fingers]
OMIM: "Tapered fingertips" [OMIM:Tapered fingertips]
OMIM: "Tapering fingers" [OMIM:Tapering fingers]
OMIM: "Tapered fingers (in some patients)" [OMIM:Tapered fingers (in some patients)]
OMIM: "Tapering fingers (in some patients)" [OMIM:Tapering fingers (in some patients)]
UMLS:C0426886 "Tapering fingers (finding)" [Orphanet:20360]
Is a (Direct Parents):
HPO         Long fingers
Orphanet Abnormality of the hand
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 digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Long fingers(HPO:0100807)
                            Tapered finger(HPO:0001182)
                   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)
MedDRA:
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)