Ivory epiphyses of the phalanges of the hand

Symptom Information:

Symptom ID: HPO:0010234
Synonyms:
Ivory epiphyses of the fingers [HPO:0010234]
Sclerotic ivory phalangeal epiphyses [HPO:0010234]
Sclerotic ivory phalangeal epiphyses [OMIM:Sclerotic ivory phalangeal epiphyses]
Quality:
Cross references:
OMIM: "Sclerotic ivory phalangeal epiphyses" [OMIM:Sclerotic ivory phalangeal epiphyses]
Is a (Direct Parents):
HPO         Abnormality of the epiphyses of the phalanges of the hand
HPO         Ivory epiphyses
HPO         Sclerosis of finger 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)
             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)
                               Ivory epiphyses of the phalanges of the hand(HPO:0010234)
                   Ivory epiphyses(HPO:0010583)
                      Ivory epiphyses of the phalanges of the hand(HPO:0010234)
             Abnormal bone structure(HPO:0003330)
                Abnormality of bone mineral density(HPO:0004348)
                   Increased bone mineral density(HPO:0011001)
                      Sclerosis of hand bone(HPO:0004054)
                         Sclerosis of finger phalanx(HPO:0100899)
                            Ivory epiphyses of the phalanges of the hand(HPO:0010234)
             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)
                               Abnormality of the epiphyses of the phalanges of the hand(HPO:0005920)
                                  Ivory epiphyses of the phalanges of the hand(HPO:0010234)
                               Sclerosis of finger phalanx(HPO:0100899)
                                  Ivory epiphyses of the phalanges of the hand(HPO:0010234)
                         Abnormality of the epiphyses of the hand(HPO:0005924)
                            Abnormality of the epiphyses of the phalanges of the hand(HPO:0005920)
                               Ivory epiphyses of the phalanges of the hand(HPO:0010234)
                      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)
                               Ivory epiphyses of the phalanges of the hand(HPO:0010234)
                   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)
                               Ivory epiphyses of the phalanges of the hand(HPO:0010234)
                            Sclerosis of finger phalanx(HPO:0100899)
                               Ivory epiphyses of the phalanges of the hand(HPO:0010234)
                   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)
                               Ivory epiphyses of the phalanges of the hand(HPO:0010234)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME B (OMIM:133540)
Cockayne syndrome (Orphanet:191)