Clinodactyly
Symptom Information:
Symptom ID: | MedDRA:10058668 | |||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |