Widely patent fontanelles and sutures

Symptom Information:

Symptom ID: HPO:0004492
Synonyms:
Widely patent fontanels and sutures [HPO:0004492]
Widely patent fontanels and sutures [OMIM:Widely patent fontanels and sutures]
Quality:
Cross references:
OMIM: "Widely patent fontanels and sutures" [OMIM:Widely patent fontanels and sutures]
Is a (Direct Parents):
HPO         Wide cranial sutures
HPO         Large fontanelles
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)
                            Large fontanelles(HPO:0000239)
                               Widely patent fontanelles and sutures(HPO:0004492)
                         Abnormality of cranial sutures(HPO:0011329)
                            Wide cranial sutures(HPO:0010537)
                               Widely patent fontanelles and sutures(HPO:0004492)
       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)
                            Widely patent fontanelles and sutures(HPO:0004492)
                      Abnormality of cranial sutures(HPO:0011329)
                         Wide cranial sutures(HPO:0010537)
                            Widely patent fontanelles and sutures(HPO:0004492)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Hereditary hypophosphatemic rickets with hypercalciuria (Orphanet:157215)
Hypocalcemic vitamin D-dependent rickets (Orphanet:289157)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Hypospadias - hypertelorism - coloboma and deafness (Orphanet:157788)
Parietal foramina with cleidocranial dysplasia (Orphanet:251290)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Renal tubular dysgenesis (Orphanet:3033)
Schinzel-Giedion syndrome (Orphanet:798)
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B (OMIM:600081)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Zellweger syndrome (Orphanet:912)