Delayed cranial suture closure
Symptom Information:
Symptom ID: | HPO:0000270 | |||||||||||||||||||||||||||||||
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 head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the skull(HPO:0000929) Abnormality of the calvaria(HPO:0002683) Abnormality of the fontanelles or cranial sutures(HPO:0000235) Abnormality of cranial sutures(HPO:0011329) Delayed cranial suture closure(HPO:0000270) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal axial skeleton morphology(HPO:0009121) Abnormality of the skull(HPO:0000929) Abnormality of the calvaria(HPO:0002683) Abnormality of the fontanelles or cranial sutures(HPO:0000235) Abnormality of cranial sutures(HPO:0011329) Delayed cranial suture closure(HPO:0000270) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue deformities (incl intervertebral disc disorders)(MedDRA:10028377) Musculoskeletal and connective tissue deformities of skull, face and buccal cavity(MedDRA:10028378) Delayed cranial suture closure(HPO:0000270) |
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Database Frequency: | 33 / 7739 | |||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
Acro-osteolysis-keloid-like lesions-premature aging syndrome | (Orphanet:363665) |
Apert syndrome | (Orphanet:87) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Bifunctional enzyme deficiency | (Orphanet:300) |
Blackfan-Diamond anemia | (Orphanet:124) |
Brachydactyly type B | (Orphanet:93383) |
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION | (OMIM:601088) |
CLEIDOCRANIAL DYSPLASIA | (OMIM:119600) |
Craniosynostosis - anal anomalies - porokeratosis | (Orphanet:85199) |
DIAMOND-BLACKFAN ANEMIA 1 | (OMIM:105650) |
Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
Frank-Ter Haar syndrome | (Orphanet:137834) |
GAPO syndrome | (Orphanet:2067) |
Greig cephalopolysyndactyly syndrome | (Orphanet:380) |
HUNTER-MACDONALD SYNDROME | (OMIM:611962) |
Intellectual deficit, X-linked - craniofacioskeletal syndrome | (Orphanet:163979) |
Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III | (OMIM:210730) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
OSTEOGENESIS IMPERFECTA, TYPE VII | (OMIM:610682) |
OSTEOGENESIS IMPERFECTA, TYPE VIII | (OMIM:610915) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
PITUITARY HORMONE DEFICIENCY, COMBINED, 1 | (OMIM:613038) |
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome | (Orphanet:276432) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
SILVER-RUSSELL SYNDROME | (OMIM:180860) |
Saethre-Chotzen syndrome | (Orphanet:794) |
Silver-Russell syndrome | (Orphanet:813) |
TENORIO SYNDROME | (OMIM:616260) |
Wrinkly skin syndrome | (Orphanet:2834) |