Hypoplastic scapulae
Symptom Information:
Symptom ID: | HPO:0000882 | ||||||||||||
Synonyms: |
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Cross references: |
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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) Aplasia/hypoplasia involving the skeleton(HPO:0009115) Aplasia/hypoplasia affecting bones of the axial skeleton(HPO:0009122) Aplasia/Hypoplasia involving bones of the thorax(HPO:0006711) Aplasia/Hypoplasia of the scapulae(HPO:0006713) Hypoplastic scapulae(HPO:0000882) Abnormal axial skeleton morphology(HPO:0009121) Aplasia/hypoplasia affecting bones of the axial skeleton(HPO:0009122) Aplasia/Hypoplasia involving bones of the thorax(HPO:0006711) Aplasia/Hypoplasia of the scapulae(HPO:0006713) Hypoplastic scapulae(HPO:0000882) Abnormality of the thorax(HPO:0000765) Abnormality of the scapula(HPO:0000782) Aplasia/Hypoplasia of the scapulae(HPO:0006713) Hypoplastic scapulae(HPO:0000882) Aplasia/Hypoplasia involving bones of the thorax(HPO:0006711) Aplasia/Hypoplasia of the scapulae(HPO:0006713) Hypoplastic scapulae(HPO:0000882) MedDRA: |
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Database Frequency: | 28 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Achondrogenesis | (Orphanet:932) |
Achondrogenesis type 1A | (Orphanet:93299) |
Acro-renal-mandibular syndrome | (Orphanet:958) |
Bartsocas-Papas syndrome | (Orphanet:1234) |
CAMPOMELIC DYSPLASIA | (OMIM:114290) |
CHILD syndrome | (Orphanet:139) |
CLEIDOCRANIAL DYSPLASIA | (OMIM:119600) |
Campomelic dysplasia | (Orphanet:140) |
Cleidocranial dysplasia | (Orphanet:1452) |
DYGGVE-MELCHIOR-CLAUSEN DISEASE | (OMIM:223800) |
Developmental malformations - deafness - dystonia | (Orphanet:79107) |
Dyggve-Melchior-Clausen disease | (Orphanet:239) |
FIBROCHONDROGENESIS 1 | (OMIM:228520) |
Fibrochondrogenesis | (Orphanet:2021) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Mucolipidosis type 2 | (Orphanet:576) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Osteoglophonic dwarfism | (Orphanet:2645) |
Pelvis-shoulder dysplasia | (Orphanet:2839) |
Pelviscapular dysplasia | (Orphanet:93333) |
Primordial short stature - microdontia - opalescent and rootless teeth | (Orphanet:46658) |
SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES | (OMIM:602471) |
SMITH-MCCORT DYSPLASIA 1 | (OMIM:607326) |
Schneckenbecken dysplasia | (Orphanet:3144) |
Short rib-polydactyly syndrome, Beemer-Langer type | (Orphanet:93268) |
Short-rib thoracic dysplasia 7 with or without polydactyly | (OMIM:614091) |
Smith-McCort dysplasia | (Orphanet:178355) |
Ulnar-mammary syndrome | (Orphanet:3138) |