Small anterior fontanelle

Symptom Information:

Symptom ID: HPO:0000237
Synonyms:
Small anterior fontanel [HPO:0000237]
Small anterior fontanel [OMIM:Small anterior fontanel]
Small anterior fontanelle [OMIM:Small anterior fontanelle]
Quality:
Cross references:
OMIM: "Small anterior fontanel" [OMIM:Small anterior fontanel]
OMIM: "Small anterior fontanelle" [OMIM:Small anterior fontanelle]
Is a (Direct Parents):
HPO         Abnormality of the anterior fontanelle
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)
                         Abnormality of the anterior fontanelle(HPO:0000236)
                            Small anterior fontanelle(HPO:0000237)
       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)
                               Small anterior fontanelle(HPO:0000237)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Ear-patella-short stature syndrome (Orphanet:2554)
FEINGOLD SYNDROME 1 (OMIM:164280)
Feingold syndrome (Orphanet:1305)
MEIER-GORLIN SYNDROME 1 (OMIM:224690)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I (OMIM:210710)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
SECKEL SYNDROME 1 (OMIM:210600)
Seckel syndrome (Orphanet:808)
Trigonocephaly - short stature - developmental delay (Orphanet:3369)