Broad phalanx

Symptom Information:

Symptom ID: HPO:0006009
Synonyms:
Broad phalanges [HPO:0006009]
Wide phalanges [HPO:0006009]
Widened phalanges [HPO:0006009]
Broad phalanges [OMIM:Broad phalanges]
Widened phalanges [OMIM:Widened phalanges]
Quality:
Cross references:
OMIM: "Broad phalanges" [OMIM:Broad phalanges]
OMIM: "Widened phalanges" [OMIM:Widened phalanges]
Is a (Direct Parents):
HPO         Short phalanx of finger
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)
                      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)
                   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)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Acromesomelic dysplasia, Maroteaux type (Orphanet:40)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Leri pleonosteosis (Orphanet:2900)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Osteoglophonic dwarfism (Orphanet:2645)
SMITH-MCCORT DYSPLASIA 2 (OMIM:615222)
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification (Orphanet:93358)
Thiemann disease, familial form (Orphanet:3314)
Trigonocephaly - bifid nose - acral anomalies (Orphanet:3368)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)
X-linked spondyloepimetaphyseal dysplasia (Orphanet:93349)