Clinodactyly

Symptom Information:

Symptom ID: MedDRA:10058668
Synonyms:
Clinodactyly [OMIM:Clinodactyly]
Clinodactyly (2nd, 3rd, 4th fingers) [OMIM:Clinodactyly (2nd, 3rd, 4th fingers)]
Clinodactyly (2nd, 4th, 4th fingers) [OMIM:Clinodactyly (2nd, 4th, 4th fingers)]
Clinodactyly (4th and 5th fingers) [OMIM:Clinodactyly (4th and 5th fingers)]
Clinodactyly (70%) [OMIM:Clinodactyly (70%)]
Clinodactyly (88%) [OMIM:Clinodactyly (88%)]
Clinodactyly (fifth finger) [OMIM:Clinodactyly (fifth finger)]
Clinodactyly (fingers II-V) [OMIM:Clinodactyly (fingers II-V)]
Clinodactyly (in 2/4 patients) [OMIM:Clinodactyly (in 2/4 patients)]
Clinodactyly (in some patients) [OMIM:Clinodactyly (in some patients)]
Clinodactyly (rare) [OMIM:Clinodactyly (rare)]
Quality:
Cross references:
OMIM: "Clinodactyly" [OMIM:Clinodactyly]
OMIM: "Clinodactyly (2nd, 3rd, 4th fingers)" [OMIM:Clinodactyly (2nd, 3rd, 4th fingers)]
OMIM: "Clinodactyly (2nd, 4th, 4th fingers)" [OMIM:Clinodactyly (2nd, 4th, 4th fingers)]
OMIM: "Clinodactyly (4th and 5th fingers)" [OMIM:Clinodactyly (4th and 5th fingers)]
OMIM: "Clinodactyly (70%)" [OMIM:Clinodactyly (70%)]
OMIM: "Clinodactyly (88%)" [OMIM:Clinodactyly (88%)]
OMIM: "Clinodactyly (fifth finger)" [OMIM:Clinodactyly (fifth finger)]
OMIM: "Clinodactyly (fingers II-V)" [OMIM:Clinodactyly (fingers II-V)]
OMIM: "Clinodactyly (in 2/4 patients)" [OMIM:Clinodactyly (in 2/4 patients)]
OMIM: "Clinodactyly (in some patients)" [OMIM:Clinodactyly (in some patients)]
OMIM: "Clinodactyly (rare)" [OMIM:Clinodactyly (rare)]
Is a (Direct Parents):
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
Is a (Whole tree): HPO:
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)
          Clinodactyly(MedDRA:10058668)
Database Frequency: 91 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
16p11.2p12.2 microdeletion syndrome (Orphanet:261211)
3q29 microdeletion syndrome (Orphanet:65286)
8q22.1 microdeletion syndrome (Orphanet:178303)
AARSKOG SYNDROME, AUTOSOMAL DOMINANT (OMIM:100050)
AARSKOG-SCOTT SYNDROME (OMIM:305400)
ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE (OMIM:201310)
ALG3-CDG (Orphanet:79321)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Antenatal multiminicore disease with arthrogryposis multiplex congenita (Orphanet:178148)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant brachyolmia (Orphanet:93304)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Autosomal recessive spastic paraplegia type 20 (Orphanet:101000)
BRACHYDACTYLY, TYPE A1 (OMIM:112500)
BRACHYDACTYLY, TYPE A1, B (OMIM:607004)
Banki syndrome (Orphanet:1228)
Blepharo-cheilo-odontic syndrome (Orphanet:1997)
Blepharophimosis-intellectual deficit syndrome, MKB type (Orphanet:293707)
Branchio-oculo-facial syndrome (Orphanet:1297)
C syndrome (Orphanet:1308)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
CARPENTER SYNDROME 1 (OMIM:201000)
COLD-INDUCED SWEATING SYNDROME 2 (OMIM:610313)
Cranioectodermal dysplasia 1 (OMIM:218330)
Craniosynostosis and dental anomalies (Orphanet:284149)
DEND syndrome (Orphanet:79134)
Distal monosomy 10q (Orphanet:96148)
ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVEFACIAL FEATURES (OMIM:609944)
Faisalabad histiocytosis (Orphanet:254707)
Frontonasal dysplasia (Orphanet:250)
Fuhrmann syndrome (Orphanet:2854)
GOMBO SYNDROME (OMIM:233270)
Goodman syndrome (Orphanet:65798)
Growth delay due to insulin-like growth factor I resistance (Orphanet:73273)
Growth delay due to insulin-like growth factor type 1 deficiency (Orphanet:73272)
H syndrome (Orphanet:168569)
Heart-hand syndrome, Slovenian type (Orphanet:168796)
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy (Orphanet:2958)
Ito hypomelanosis (Orphanet:435)
KBG syndrome (Orphanet:2332)
Larsen-like osseous dysplasia - short stature (Orphanet:2370)
MICROPHTHALMIA, SYNDROMIC 1 (OMIM:309800)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 (OMIM:614114)
MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
McDonough syndrome (Orphanet:2471)
Meckel syndrome, type 1 (OMIM:249000)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
Microcephalic primordial dwarfism, Toriello type (Orphanet:2643)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Miller-Dieker syndrome (Orphanet:531)
Moebius syndrome (Orphanet:570)
Monosomy 18p (Orphanet:1598)
Muenke syndrome (Orphanet:53271)
Myhre syndrome (Orphanet:2588)
NOONAN SYNDROME 1 (OMIM:163950)
Nager syndrome (Orphanet:245)
Neu-Laxova syndrome (Orphanet:2671)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
OROFACIODIGITAL SYNDROME VI (OMIM:277170)
OSLAM syndrome (Orphanet:2760)
OTOFACIOCERVICAL SYNDROME 2 (OMIM:615560)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Paris-Trousseau thrombocytopenia (Orphanet:851)
Permanent neonatal diabetes mellitus (Orphanet:99885)
Pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome (Orphanet:254723)
Pitt-Hopkins syndrome (Orphanet:2896)
Prader-Willi syndrome (Orphanet:739)
Pseudoaminopterin syndrome (Orphanet:221120)
ROBERTS SYNDROME (OMIM:268300)
Rosaï-Dorfman disease (Orphanet:158014)
SC PHOCOMELIA SYNDROME (OMIM:269000)
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY (OMIM:181405)
SHORT syndrome (Orphanet:3163)
Schilbach-Rott syndrome (Orphanet:2353)
Short stature - valvular heart disease - characteristic facies (Orphanet:2868)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Simpson-Golabi-Behmel syndrome type 2 (Orphanet:79022)
Spondyloepiphyseal dysplasia, MacDermot type (Orphanet:163668)
Syndromic multisystem autoimmune disease due to Itch deficiency (Orphanet:228426)
TARSAL-CARPAL COALITION SYNDROME (OMIM:186570)
THREE M SYNDROME 1 (OMIM:273750)
Temtamy preaxial brachydactyly syndrome (Orphanet:363417)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
W syndrome (Orphanet:2804)
Waardenburg syndrome type 3 (Orphanet:896)
Weaver syndrome (Orphanet:3447)