Delayed closure of the anterior fontanelle
Symptom Information:
Symptom ID: | HPO:0001476 | |||||||||||||||||||||
Synonyms: |
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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 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 fontanelles(HPO:0011328) Abnormality of the anterior fontanelle(HPO:0000236) Delayed closure of the anterior fontanelle(HPO:0001476) Abnormality of cranial sutures(HPO:0011329) Delayed cranial suture closure(HPO:0000270) Delayed closure of the anterior fontanelle(HPO:0001476) 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 fontanelles(HPO:0011328) Abnormality of the anterior fontanelle(HPO:0000236) Delayed closure of the anterior fontanelle(HPO:0001476) Abnormality of cranial sutures(HPO:0011329) Delayed cranial suture closure(HPO:0000270) Delayed closure of the anterior fontanelle(HPO:0001476) 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 closure of the anterior fontanelle(HPO:0001476) |
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Database Frequency: | 23 / 7739 | |||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
Autosomal dominant Kenny-Caffey syndrome | (Orphanet:93325) |
Autosomal recessive Kenny-Caffey syndrome | (Orphanet:93324) |
Canavan disease | (Orphanet:141) |
Coffin-Lowry syndrome | (Orphanet:192) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
Dysosteosclerosis | (Orphanet:1782) |
Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
Intellectual deficit, X-linked - craniofacioskeletal syndrome | (Orphanet:163979) |
Kenny-Caffey syndrome | (Orphanet:2333) |
Mesomelic dysplasia, Savarirayan type | (Orphanet:85170) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
Nestor-Guillermo progeria syndrome | (Orphanet:280576) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
Otopalatodigital syndrome | (Orphanet:669) |
Otopalatodigital syndrome type 1 | (Orphanet:90650) |
Otopalatodigital syndrome type 2 | (Orphanet:90652) |
PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER) | (OMIM:614886) |
PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER) | (OMIM:614887) |
Suarez-Stickler syndrome | (Orphanet:166277) |
Torg-Winchester syndrome | (Orphanet:3460) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |