Macrodactyly

Symptom Information:

Symptom ID: HPO:0004099
Synonyms:
Finger overgrowth [HPO:0004099]
Megalodactyly [HPO:0004099]
macrodactyly [HPO:0004099]
Macrodactyly [OMIM:Macrodactyly]
Macrodactyly [MedDRA:10025386]
Macrodactylia (fingers) [MedDRA:10025386]
Macrodactylia of toes [MedDRA:10025386]
Macrodactyly (in some patients) [OMIM:Macrodactyly (in some patients)]
Quality:
Cross references:
OMIM: "Macrodactyly" [OMIM:Macrodactyly]
OMIM: "Macrodactyly (in some patients)" [OMIM:Macrodactyly (in some patients)]
UMLS:C2117323 "macrodactyly" [HPO:0004099]
Is a (Direct Parents):
HPO         Abnormality of digit
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
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)
                      Macrodactyly(HPO:0004099)
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)
          Macrodactyly(HPO:0004099)
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Angio-osteohypertrophic syndrome (Orphanet:2346)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
CLOVE syndrome (Orphanet:140944)
Klippel-Trénaunay syndrome (Orphanet:90308)
MEGALODACTYLY (OMIM:155500)