Wide anterior fontanel

Symptom Information:

Symptom ID: HPO:0000260
Synonyms:
Large anterior fontanel [HPO:0000260]
Large anterior fontanelle [HPO:0000260]
LARGE ANTERIOR FONTANELS [HPO:0000260]
Large open anterior fontanel [HPO:0000260]
Large open anterior fontanelle [HPO:0000260]
Wide anterior fontanelle [HPO:0000260]
Wide open anterior fontanelle [HPO:0000260]
Large fontanelle [Orphanet:2440]
Large fontanelle (finding) [Orphanet:2440]
Delayed fontanelle closure [Orphanet:2440]
Large anterior fontanel [OMIM:Large anterior fontanel]
Large anterior fontanelle [OMIM:Large anterior fontanelle]
Large open anterior fontanel [OMIM:Large open anterior fontanel]
Large open anterior fontanelle [OMIM:Large open anterior fontanelle]
Wide anterior fontanel [OMIM:Wide anterior fontanel]
Wide anterior fontanelle [OMIM:Wide anterior fontanelle]
Wide open anterior fontanelle [OMIM:Wide open anterior fontanelle]
Large fontanelle/delayed fontanelle closure [Orphanet:2440]
Enlarged fontanelle [Orphanet:2440]
Delayed fontanelle closure [MedDRA:10054034]
Enlarged fontanelle [MedDRA:10054034]
Enlarged fontanelle [OMIM:Enlarged fontanelle]
Large anterior fontanel (birth) [OMIM:Large anterior fontanel (birth)]
Large anterior fontanels [OMIM:Large anterior fontanels]
Large fontanelles (male and females) [OMIM:Large fontanelles (male and females)]
Quality:
Cross references:
HPO:0001476 "Delayed closure of the anterior fontanelle" [Orphanet:2440]
HPO:0000239 "Large fontanelles" [Orphanet:2440]
HPO:0000270 "Delayed cranial suture closure" [Orphanet:2440]
Orphanet:2440 "Large fontanelle/delayed fontanelle closure" [Orphanet:2440]
OMIM: "Large anterior fontanel" [OMIM:Large anterior fontanel]
OMIM: "Large anterior fontanelle" [OMIM:Large anterior fontanelle]
OMIM: "Large open anterior fontanel" [OMIM:Large open anterior fontanel]
OMIM: "Large open anterior fontanelle" [OMIM:Large open anterior fontanelle]
OMIM: "Wide anterior fontanel" [OMIM:Wide anterior fontanel]
OMIM: "Wide anterior fontanelle" [OMIM:Wide anterior fontanelle]
OMIM: "Wide open anterior fontanelle" [OMIM:Wide open anterior fontanelle]
OMIM: "Enlarged fontanelle" [OMIM:Enlarged fontanelle]
OMIM: "Large anterior fontanel (birth)" [OMIM:Large anterior fontanel (birth)]
OMIM: "Large anterior fontanels" [OMIM:Large anterior fontanels]
OMIM: "Large fontanelles (male and females)" [OMIM:Large fontanelles (male and females)]
UMLS:C1096211 "Delayed fontanelle closure" [Orphanet:2440]
UMLS:C0456132 "Large fontanelle" [Orphanet:2440]
Is a (Direct Parents):
HPO         Large fontanelles
HPO         Abnormality of the anterior fontanelle
Orphanet Abnormality of the skull
MedDRA Musculoskeletal and connective tissue deformities of skull, face and buccal cavity
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 fontanelles(HPO:0011328)
                         Large fontanelles(HPO:0000239)
                            Wide anterior fontanel(HPO:0000260)
                         Abnormality of the anterior fontanelle(HPO:0000236)
                            Wide anterior fontanel(HPO:0000260)
       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)
                            Large fontanelles(HPO:0000239)
                               Wide anterior fontanel(HPO:0000260)
                            Abnormality of the anterior fontanelle(HPO:0000236)
                               Wide anterior fontanel(HPO:0000260)
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)
          Wide anterior fontanel(HPO:0000260)
Database Frequency: 55 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
3MC SYNDROME 1 (OMIM:257920)
AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA (OMIM:613623)
Acrocallosal syndrome (Orphanet:36)
Acrofacial dysostosis, Rodriguez type (Orphanet:1788)
Antley-Bixler syndrome (Orphanet:83)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive cutis laxa type 2, classic type (Orphanet:357074)
Autosomal recessive cutis laxa type 2A (Orphanet:357058)
Brachydactyly type B (Orphanet:93383)
CAMPOMELIC DYSPLASIA (OMIM:114290)
CHROMOSOME 16q22 DELETION SYNDROME (OMIM:614541)
CRANIOMETADIAPHYSEAL DYSPLASIA (OMIM:269300)
Campomelic dysplasia (Orphanet:140)
Cerebro-facio-articular syndrome (Orphanet:314679)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
Costello syndrome (Orphanet:3071)
Craniolenticulosutural dysplasia (Orphanet:50814)
Craniometadiaphyseal dysplasia, wormian bone type (Orphanet:85184)
Donnai-Barrow syndrome (Orphanet:2143)
Dyssegmental dysplasia - glaucoma (Orphanet:1804)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
FIBROCHONDROGENESIS 1 (OMIM:228520)
Fibrochondrogenesis (Orphanet:2021)
Frank-Ter Haar syndrome (Orphanet:137834)
GAPO syndrome (Orphanet:2067)
Gómez-López-Hernández syndrome (Orphanet:1532)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
Isolated thyroid-stimulating hormone deficiency (Orphanet:90674)
LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE (OMIM:601356)
Larsen-like osseous dysplasia - short stature (Orphanet:2370)
Lethal Kniest-like dysplasia (Orphanet:2347)
Marden-Walker syndrome (Orphanet:2461)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 (Orphanet:300496)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
OSTEOGENESIS IMPERFECTA, TYPE III (OMIM:259420)
OSTEOGENESIS IMPERFECTA, TYPE VII (OMIM:610682)
OSTEOGENESIS IMPERFECTA, TYPE VIII (OMIM:610915)
Osteogenesis imperfecta type 3 (Orphanet:216812)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 2 (Orphanet:90652)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Peters-plus syndrome (Orphanet:709)
Rhizomelic syndrome, Urbach type (Orphanet:3098)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
SENER SYNDROME (OMIM:606156)
Shprintzen-Goldberg syndrome (Orphanet:2462)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
Wrinkly skin syndrome (Orphanet:2834)
X-linked lissencephaly with abnormal genitalia (Orphanet:452)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)