Cutaneous finger syndactyly

Symptom Information:

Symptom ID: HPO:0010554
Synonyms:
Cutaneous syndactyly [HPO:0010554]
Cutaneous syndactyly (hands) [HPO:0010554]
Cutaneous syndactyly of fingers [HPO:0010554]
Syndactyly, cutaneous [HPO:0010554]
Cutaneous syndactyly of fingers [Orphanet:20440]
Simple syndactyly of fingers (disorder) [Orphanet:20440]
Cutaneous syndactyly [OMIM:Cutaneous syndactyly]
Syndactyly, cutaneous [OMIM:Syndactyly, cutaneous]
Syndactyly of fingers/interdigital palm [Orphanet:20440]
Cutaneous syndactyly (2,3,4) [OMIM:Cutaneous syndactyly (2,3,4)]
Cutaneous syndactyly (2nd-3rd, 4th-5th) [OMIM:Cutaneous syndactyly (2nd-3rd, 4th-5th)]
Cutaneous syndactyly (digits 2nd-5th) [OMIM:Cutaneous syndactyly (digits 2nd-5th)]
Cutaneous syndactyly (fingers 2,3,4,5) [OMIM:Cutaneous syndactyly (fingers 2,3,4,5)]
Cutaneous syndactyly (in some patients) [OMIM:Cutaneous syndactyly (in some patients)]
Cutaneous syndactyly (less common) [OMIM:Cutaneous syndactyly (less common)]
Cutaneous syndactyly (toes 2-3) [OMIM:Cutaneous syndactyly (toes 2-3)]
Quality:
Cross references:
Orphanet:20440 "Syndactyly of fingers/interdigital palm" [Orphanet:20440]
OMIM: "Cutaneous syndactyly" [OMIM:Cutaneous syndactyly]
OMIM: "Syndactyly, cutaneous" [OMIM:Syndactyly, cutaneous]
OMIM: "Cutaneous syndactyly (2,3,4)" [OMIM:Cutaneous syndactyly (2,3,4)]
OMIM: "Cutaneous syndactyly (2nd-3rd, 4th-5th)" [OMIM:Cutaneous syndactyly (2nd-3rd, 4th-5th)]
OMIM: "Cutaneous syndactyly (digits 2nd-5th)" [OMIM:Cutaneous syndactyly (digits 2nd-5th)]
OMIM: "Cutaneous syndactyly (fingers 2,3,4,5)" [OMIM:Cutaneous syndactyly (fingers 2,3,4,5)]
OMIM: "Cutaneous syndactyly (in some patients)" [OMIM:Cutaneous syndactyly (in some patients)]
OMIM: "Cutaneous syndactyly (less common)" [OMIM:Cutaneous syndactyly (less common)]
OMIM: "Cutaneous syndactyly (toes 2-3)" [OMIM:Cutaneous syndactyly (toes 2-3)]
Is a (Direct Parents):
Orphanet Abnormality of the hand
HPO         Finger syndactyly
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)
                      Syndactyly(HPO:0001159)
                         Finger syndactyly(HPO:0006101)
                            Cutaneous finger syndactyly(HPO:0010554)
MedDRA:
Database Frequency: 39 / 7739
Resource:

All diseases associated with this symptom:

19q13.11 microdeletion syndrome (Orphanet:217346)
Acrofacial dysostosis, Palagonia type (Orphanet:1787)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Apert syndrome (Orphanet:87)
Aphalangy - syndactyly - microcephaly (Orphanet:1113)
Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)
BARATELA-SCOTT SYNDROME (OMIM:300881)
Bardet-Biedl syndrome (Orphanet:110)
Blepharophimosis - ptosis - esotropia - syndactyly - short stature (Orphanet:2057)
Bloom syndrome (Orphanet:125)
Brachydactyly type B (Orphanet:93383)
Brachydactyly type B2 (Orphanet:140908)
CARPENTER SYNDROME 2 (OMIM:614976)
CREE MENTAL RETARDATION SYNDROME (OMIM:606851)
Cerebro-facio-articular syndrome (Orphanet:314679)
Cranioectodermal dysplasia 4 (OMIM:614378)
Ear-patella-short stature syndrome (Orphanet:2554)
Ectodermal dysplasia - syndactyly syndrome (Orphanet:247820)
Fraser syndrome (Orphanet:2052)
Gordon syndrome (Orphanet:376)
Hennekam syndrome (Orphanet:2136)
MEIER-GORLIN SYNDROME 1 (OMIM:224690)
MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
Mowat-Wilson syndrome (Orphanet:2152)
Multiple synostoses syndrome (Orphanet:3237)
POLYDACTYLY, POSTAXIAL, TYPE A5 (OMIM:263450)
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES (OMIM:602249)
Roifman syndrome (Orphanet:353298)
Rosselli-Gulienetti syndrome (Orphanet:90339)
SCLEROSTEOSIS 2 (OMIM:614305)
Split hand - urinary anomalies - spina bifida (Orphanet:2437)
Symphalangism with multiple anomalies of hands and feet (Orphanet:3246)
Syndactyly type 5 (Orphanet:93406)
Timothy syndrome (Orphanet:65283)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
Waardenburg syndrome (Orphanet:3440)
Waardenburg syndrome type 3 (Orphanet:896)
Zlotogora-Ogur syndrome (Orphanet:3253)