Decreased skull ossification
Symptom Information:
Symptom ID: | HPO:0004331 | ||||||||||||||
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) Abnormal bone structure(HPO:0003330) Abnormal bone ossification(HPO:0011849) Decreased skull ossification(HPO:0004331) Abnormal axial skeleton morphology(HPO:0009121) Abnormality of the skull(HPO:0000929) Abnormality of skull ossification(HPO:0002703) Decreased skull ossification(HPO:0004331) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the skull(HPO:0000929) Abnormality of skull ossification(HPO:0002703) Decreased skull ossification(HPO:0004331) MedDRA: |
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Database Frequency: | 31 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
Achondrogenesis | (Orphanet:932) |
Achondrogenesis type 1A | (Orphanet:93299) |
Acroosteolysis, dominant type | (Orphanet:955) |
Amish lethal microcephaly | (Orphanet:99742) |
Arachnodactyly - abnormal ossification - intellectual deficit | (Orphanet:1129) |
Autosomal recessive Kenny-Caffey syndrome | (Orphanet:93324) |
Cleidocranial dysplasia | (Orphanet:1452) |
Cloverleaf skull - multiple congenital anomalies | (Orphanet:93267) |
Congenital amegakaryocytic thrombocytopenia | (Orphanet:3319) |
Congenital osteogenesis imperfecta - microcephaly - cataracts | (Orphanet:2772) |
Crane-Heise syndrome | (Orphanet:1512) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
Craniomicromelic syndrome | (Orphanet:1524) |
Delayed membranous cranial ossification | (Orphanet:3034) |
Diaphragmatic defect - limb deficiency - skull defect | (Orphanet:2141) |
GAPO syndrome | (Orphanet:2067) |
Grant syndrome | (Orphanet:2097) |
Greenberg dysplasia | (Orphanet:1426) |
Infantile hypophosphatasia | (Orphanet:247651) |
Lethal restrictive dermopathy | (Orphanet:1662) |
OSTEOGENESIS IMPERFECTA, TYPE VIII | (OMIM:610915) |
Osteocraniostenosis | (Orphanet:2763) |
Osteogenesis imperfecta | (Orphanet:666) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Potocki-Shaffer syndrome | (Orphanet:52022) |
Progeroid syndrome, Petty type | (Orphanet:2963) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Short rib-polydactyly syndrome | (Orphanet:1505) |
Triploidy | (Orphanet:3376) |
X-linked dominant chondrodysplasia, Chassaing-Lacombe type | (Orphanet:163966) |
Yunis-Varon syndrome | (Orphanet:3472) |