Oligodactyly

Symptom Information:

Symptom ID: HPO:0012165
Synonyms:
Oligodactyly [OMIM:Oligodactyly]
Oligodactyly (45%) [OMIM:Oligodactyly (45%)]
Quality:
Cross references:
OMIM: "Oligodactyly" [OMIM:Oligodactyly]
OMIM: "Oligodactyly (45%)" [OMIM:Oligodactyly (45%)]
Is a (Direct Parents):
HPO         Abnormality of digit
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)
                      Oligodactyly(HPO:0012165)
MedDRA:
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Acrofacial dysostosis, Rodriguez type (Orphanet:1788)
CHROMOSOME 17p13.3, TELOMERIC, DUPLICATION SYNDROME (OMIM:612576)
CORNELIA DE LANGE SYNDROME 1 (OMIM:122470)
Focal dermal hypoplasia (Orphanet:2092)
Fuhrmann syndrome (Orphanet:2854)
Klippel-Trénaunay syndrome (Orphanet:90308)
Lethal occipital encephalocele-skeletal dysplasia syndrome (Orphanet:293925)
Microgastria - limb reduction defect (Orphanet:2538)
Microphthalmia with limb anomalies (Orphanet:1106)
Orofaciodigital syndrome type 10 (Orphanet:2756)
Pallister-Hall syndrome (Orphanet:672)
Phocomelia, Schinzel type (Orphanet:2879)
ROBERTS SYNDROME (OMIM:268300)
Robin sequence - oligodactyly (Orphanet:3104)
SANTOS SYNDROME (OMIM:613005)
ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS (OMIM:276822)
WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME (OMIM:602418)
XK aprosencephaly (Orphanet:3469)