Premature loss of primary teeth

Symptom Information:

Symptom ID: HPO:0006323
Synonyms:
Premature deciduous tooth loss [HPO:0006323]
Premature loss of deciduous teeth [HPO:0006323]
Premature loss of deciduous tooth [Orphanet:12750]
Premature loss of deciduous teeth [OMIM:Premature loss of deciduous teeth]
Premature loss of primary teeth [OMIM:Premature loss of primary teeth]
Premature lost of decidious teeth [Orphanet:12750]
Premature deciduous tooth loss (less than five years of age) [OMIM:Premature deciduous tooth loss (less than five years of age)]
Quality:
Cross references:
Orphanet:12750 "Premature lost of decidious teeth" [Orphanet:12750]
OMIM: "Premature loss of deciduous teeth" [OMIM:Premature loss of deciduous teeth]
OMIM: "Premature loss of primary teeth" [OMIM:Premature loss of primary teeth]
OMIM: "Premature deciduous tooth loss (less than five years of age)" [OMIM:Premature deciduous tooth loss (less than five years of age)]
Is a (Direct Parents):
HPO         Premature loss of teeth
HPO         Abnormality of primary teeth
Orphanet Abnormality of the teeth
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 face(HPO:0000271)
                Abnormality of the mouth(HPO:0000153)
                   Abnormality of the oral cavity(HPO:0000163)
                      Abnormality of the teeth(HPO:0000164)
                         Abnormality of primary teeth(HPO:0006481)
                            Premature loss of primary teeth(HPO:0006323)
                         Premature loss of teeth(HPO:0006480)
                            Premature loss of primary teeth(HPO:0006323)
MedDRA:
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Adult hypophosphatasia (Orphanet:247676)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Childhood-onset hypophosphatasia (Orphanet:247667)
Ehlers-Danlos syndrome, periodontitis type (Orphanet:75392)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Infantile hypophosphatasia (Orphanet:247651)
Kindler syndrome (Orphanet:2908)
Oculodentodigital dysplasia (Orphanet:2710)
Odontohypophosphatasia (Orphanet:247685)
Odontomicronychial dysplasia (Orphanet:1811)
Papillon-Lefèvre syndrome (Orphanet:678)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Schöpf-Schulz-Passarge syndrome (Orphanet:50944)
Yunis-Varon syndrome (Orphanet:3472)