Cone-shaped epiphyses of the phalanges of the hand
Symptom Information:
Symptom ID: | HPO:0010230 | ||||||||||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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 the epiphyses of the hand(HPO:0005924) Abnormality of the epiphyses of the phalanges of the hand(HPO:0005920) Cone-shaped epiphyses of the phalanges of the hand(HPO:0010230) Abnormality of finger(HPO:0001167) Abnormality of phalanx of finger(HPO:0005918) Abnormality of the epiphyses of the phalanges of the hand(HPO:0005920) Cone-shaped epiphyses of the phalanges of the hand(HPO:0010230) 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) Cone-shaped epiphyses of the phalanges of the hand(HPO:0010230) 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) Cone-shaped epiphyses of the phalanges of the hand(HPO:0010230) 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) Cone-shaped epiphyses of the phalanges of the hand(HPO:0010230) 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) Cone-shaped epiphyses of the phalanges of the hand(HPO:0010230) Cone-shaped epiphysis(HPO:0010579) Cone-shaped epiphyses of the phalanges of the hand(HPO:0010230) MedDRA: |
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Database Frequency: | 34 / 7739 | ||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acrocapitofemoral dysplasia | (Orphanet:63446) |
Acrodysostosis with multiple hormone resistance | (Orphanet:280651) |
Acromesomelic dysplasia, Maroteaux type | (Orphanet:40) |
BRACHYDACTYLY, TYPE A1, B | (OMIM:607004) |
CLEIDOCRANIAL DYSPLASIA | (OMIM:119600) |
CRANIOSYNOSTOSIS, ADELAIDE TYPE | (OMIM:600593) |
Cleidocranial dysplasia | (Orphanet:1452) |
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED | (OMIM:304950) |
Dyggve-Melchior-Clausen disease | (Orphanet:239) |
Floating-Harbor syndrome | (Orphanet:2044) |
Goldblatt syndrome | (Orphanet:166272) |
Jeune syndrome | (Orphanet:474) |
Langer-Giedion syndrome | (Orphanet:502) |
MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES | (OMIM:606772) |
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS | (OMIM:250460) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III | (OMIM:210730) |
Metaphyseal acroscyphodysplasia | (Orphanet:1240) |
Metaphyseal chondrodysplasia, Kaitila type | (Orphanet:166038) |
Muenke syndrome | (Orphanet:53271) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Paraplegia - brachydactyly - cone-shaped epiphysis | (Orphanet:2823) |
Peripheral dysostosis | (Orphanet:1795) |
Postaxial tetramelic oligodactyly | (Orphanet:2730) |
SECKEL SYNDROME 1 | (OMIM:210600) |
SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS | (OMIM:609616) |
Saldino-Mainzer syndrome | (Orphanet:140969) |
Seckel syndrome | (Orphanet:808) |
Short-rib thoracic dysplasia 1 with or without polydactyly | (OMIM:208500) |
Short-rib thoracic dysplasia 10 with or without polydactyly | (OMIM:615630) |
Spondylometaphyseal dysplasia, Sedaghatian type | (Orphanet:93317) |
Spondyloperipheral dysplasia - short ulna | (Orphanet:1856) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE III | (OMIM:190351) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
X-linked spondyloepimetaphyseal dysplasia | (Orphanet:93349) |