Premature fusion of phalangeal epiphyses

Symptom Information:

Symptom ID: HPO:0006140
Synonyms:
Premature fusion of phalangeal epiphyses [OMIM:Premature fusion of phalangeal epiphyses]
Quality:
Cross references:
OMIM: "Premature fusion of phalangeal epiphyses" [OMIM:Premature fusion of phalangeal epiphyses]
Is a (Direct Parents):
HPO         Abnormality of the epiphyses of the phalanges of the hand
HPO         Abnormal epiphyseal ossification
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 limb epiphysis morphology(HPO:0006505)
                      Abnormality of upper limb epiphysis morphology(HPO:0003839)
                         Abnormality of the epiphyses of the hand(HPO:0005924)
                            Abnormality of the epiphyses of the phalanges of the hand(HPO:0005920)
                               Premature fusion of phalangeal epiphyses(HPO:0006140)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Abnormality of phalanx of finger(HPO:0005918)
                            Abnormality of the epiphyses of the phalanges of the hand(HPO:0005920)
                               Premature fusion of phalangeal epiphyses(HPO:0006140)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of upper limb epiphysis morphology(HPO:0003839)
                         Abnormality of the epiphyses of the hand(HPO:0005924)
                            Abnormality of the epiphyses of the phalanges of the hand(HPO:0005920)
                               Premature fusion of phalangeal epiphyses(HPO:0006140)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of finger(HPO:0001167)
                            Abnormality of phalanx of finger(HPO:0005918)
                               Abnormality of the epiphyses of the phalanges of the hand(HPO:0005920)
                                  Premature fusion of phalangeal epiphyses(HPO:0006140)
                         Abnormality of the epiphyses of the hand(HPO:0005924)
                            Abnormality of the epiphyses of the phalanges of the hand(HPO:0005920)
                               Premature fusion of phalangeal epiphyses(HPO:0006140)
             Abnormal bone structure(HPO:0003330)
                Abnormal bone ossification(HPO:0011849)
                   Abnormal epiphyseal ossification(HPO:0010656)
                      Premature fusion of phalangeal epiphyses(HPO:0006140)
             Abnormality of long bone morphology(HPO:0011314)
                Abnormality of epiphysis morphology(HPO:0005930)
                   Abnormality of limb epiphysis morphology(HPO:0006505)
                      Abnormality of upper limb epiphysis morphology(HPO:0003839)
                         Abnormality of the epiphyses of the hand(HPO:0005924)
                            Abnormality of the epiphyses of the phalanges of the hand(HPO:0005920)
                               Premature fusion of phalangeal epiphyses(HPO:0006140)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Keutel syndrome (Orphanet:85202)