Broad phalanges of the hand

Symptom Information:

Symptom ID: HPO:0009768
Synonyms:
Widening of phalanges of the hand [HPO:0009768]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Broad finger
HPO         Broad phalanx
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 the upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of finger(HPO:0001167)
                            Abnormality of phalanx of finger(HPO:0005918)
                               Aplasia/Hypoplasia of the phalanges of the hand(HPO:0009767)
                                  Short phalanx of finger(HPO:0009803)
                                     Broad phalanx(HPO:0006009)
                                        Broad phalanges of the hand(HPO:0009768)
                            Broad finger(HPO:0001500)
                               Broad phalanges of the hand(HPO:0009768)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Abnormality of phalanx of finger(HPO:0005918)
                            Aplasia/Hypoplasia of the phalanges of the hand(HPO:0009767)
                               Short phalanx of finger(HPO:0009803)
                                  Broad phalanx(HPO:0006009)
                                     Broad phalanges of the hand(HPO:0009768)
                         Broad finger(HPO:0001500)
                            Broad phalanges of the hand(HPO:0009768)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Frontometaphyseal dysplasia (Orphanet:1826)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Weill-Marchesani syndrome (Orphanet:3449)