Delayed cranial suture closure

Symptom Information:

Symptom ID: HPO:0000270
Synonyms:
Broad late closing cranial sutures [HPO:0000270]
Delayed closure of fontanel [HPO:0000270]
Delayed closure of fontanelles [HPO:0000270]
Delayed closure of the fontanelles [HPO:0000270]
Delayed fontanel closure [HPO:0000270]
Delayed fontanelle closure [HPO:0000270]
Late closing fontanelles [HPO:0000270]
Late closure of fontanelle [HPO:0000270]
Late-closing fontanelle [HPO:0000270]
Open sutures [HPO:0000270]
Large fontanelle [Orphanet:2440]
Large fontanelle (finding) [Orphanet:2440]
Delayed fontanelle closure [Orphanet:2440]
Broad late closing cranial sutures [OMIM:Broad late closing cranial sutures]
Delayed closure of fontanel [OMIM:Delayed closure of fontanel]
Delayed closure of fontanelles [OMIM:Delayed closure of fontanelles]
Delayed closure of the fontanelles [OMIM:Delayed closure of the fontanelles]
Delayed fontanel closure [OMIM:Delayed fontanel closure]
Delayed fontanelle closure [OMIM:Delayed fontanelle closure]
Late closing fontanelles [OMIM:Late closing fontanelles]
Late closure of fontanelle [OMIM:Late closure of fontanelle]
Open sutures [OMIM:Open sutures]
Large fontanelle/delayed fontanelle closure [Orphanet:2440]
Enlarged fontanelle [Orphanet:2440]
Delayed fontanelle closure [MedDRA:10054034]
Enlarged fontanelle [MedDRA:10054034]
Delayed closure of fontanelle [OMIM:Delayed closure of fontanelle]
Delayed closure of fontanels [OMIM:Delayed closure of fontanels]
Enlarged fontanelle [OMIM:Enlarged fontanelle]
Large fontanelles (male and females) [OMIM:Large fontanelles (male and females)]
Open sutures (untreated hypothyroidism) [OMIM:Open sutures (untreated hypothyroidism)]
Quality:
Cross references:
HPO:0001476 "Delayed closure of the anterior fontanelle" [Orphanet:2440]
HPO:0000239 "Large fontanelles" [Orphanet:2440]
HPO:0000260 "Wide anterior fontanel" [Orphanet:2440]
Orphanet:2440 "Large fontanelle/delayed fontanelle closure" [Orphanet:2440]
OMIM: "Broad late closing cranial sutures" [OMIM:Broad late closing cranial sutures]
OMIM: "Delayed closure of fontanel" [OMIM:Delayed closure of fontanel]
OMIM: "Delayed closure of fontanelles" [OMIM:Delayed closure of fontanelles]
OMIM: "Delayed closure of the fontanelles" [OMIM:Delayed closure of the fontanelles]
OMIM: "Delayed fontanel closure" [OMIM:Delayed fontanel closure]
OMIM: "Delayed fontanelle closure" [OMIM:Delayed fontanelle closure]
OMIM: "Late closing fontanelles" [OMIM:Late closing fontanelles]
OMIM: "Late closure of fontanelle" [OMIM:Late closure of fontanelle]
OMIM: "Open sutures" [OMIM:Open sutures]
OMIM: "Delayed closure of fontanelle" [OMIM:Delayed closure of fontanelle]
OMIM: "Delayed closure of fontanels" [OMIM:Delayed closure of fontanels]
OMIM: "Enlarged fontanelle" [OMIM:Enlarged fontanelle]
OMIM: "Large fontanelles (male and females)" [OMIM:Large fontanelles (male and females)]
OMIM: "Open sutures (untreated hypothyroidism)" [OMIM:Open sutures (untreated hypothyroidism)]
UMLS:C1096211 "Delayed fontanelle closure" [Orphanet:2440]
UMLS:C0456132 "Large fontanelle" [Orphanet:2440]
Is a (Direct Parents):
HPO         Abnormality of cranial sutures
MedDRA Musculoskeletal and connective tissue deformities of skull, face and buccal cavity
Orphanet Abnormality of the skull
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 cranial sutures(HPO:0011329)
                            Delayed cranial suture closure(HPO:0000270)
       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)
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)
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)