Abnormality of the mouth

Symptom Information:

Symptom ID: HPO:0000153
Synonyms:
Mouth anomaly [Orphanet:9000]
Congenital anomaly of mouth (disorder) [Orphanet:9000]
Mouth Abnormalities [Orphanet:9000]
Anomalies of mouth, lip and philtrum [Orphanet:9000]
Congenital oral malformation [Orphanet:9000]
Congenital oral malformation [MedDRA:10061070]
Congenital mouth malformation NOS [MedDRA:10061070]
Congenital oral malformation NOS [MedDRA:10061070]
Other specified congenital anomalies of mouth [MedDRA:10061070]
Other specified congenital anomalies of mouth and pharynx [MedDRA:10061070]
Anomaly of mouth, lip and philtrum [Orphanet:9000]
Quality:
Cross references:
Orphanet:9000 "Anomalies of mouth, lip and philtrum" [Orphanet:9000]
UMLS:C0026633 "Mouth Abnormalities" [Orphanet:9000]
Is a (Direct Parents):
HPO         Abnormality of the mouth floor
HPO         Abnormality of the face
HPO         Abnormality of mandible condylar process
MedDRA Oral cavity disorders congenital NEC
HPO         Abnormality of mandibular ramus
HPO         Abnormality of inferior alveolar artery
HPO         Abnormality of mandible coronoid process
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)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Gastrointestinal tract disorders congenital(MedDRA:10018018)
       Oral cavity disorders congenital NEC(MedDRA:10030967)
          Abnormality of the mouth(HPO:0000153)
Database Frequency: 60 / 7739
Resource:

All diseases associated with this symptom:

AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA, WITH MENTAL RETARDATION (OMIM:204850)
Acromegaloid facial appearance syndrome (Orphanet:965)
Arachnodactyly - intellectual deficit - dysmorphism (Orphanet:1130)
Arthrogryposis multiplex congenita - whistling face (Orphanet:1150)
Ascher syndrome (Orphanet:1253)
Bartsocas-Papas syndrome (Orphanet:1234)
Bazex-Dupré-Christol syndrome (Orphanet:113)
Blue rubber bleb nevus (Orphanet:1059)
Cardiocranial syndrome, Pfeiffer type (Orphanet:2872)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Cleft palate-lateral synechia syndrome (Orphanet:2016)
Congenital erythropoietic porphyria (Orphanet:79277)
Congenital unilateral hypoplasia of depressor anguli oris (Orphanet:1166)
Cutis laxa (Orphanet:209)
Cyclic neutropenia (Orphanet:2686)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Epidermolysis bullosa simplex with anodontia/hypodontia (Orphanet:2325)
FOCAL EPITHELIAL HYPERPLASIA OF THE ORAL MUCOSA (OMIM:136400)
FOCAL EPITHELIAL HYPERPLASIA, ORAL (OMIM:229045)
Focal facial dermal dysplasia (Orphanet:79133)
Freeman-Sheldon syndrome (Orphanet:2053)
Growth hormone insensitivity syndrome (Orphanet:181393)
Harlequin ichthyosis (Orphanet:457)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Holoprosencephaly (Orphanet:2162)
Hypertrichosis (Orphanet:79365)
Imperforate oropharynx - costo vetebral anomalies (Orphanet:2759)
Kennedy disease (Orphanet:481)
LIP, HAMARTOMATOUS (OMIM:151640)
Macrostomia - preauricular tags - external ophthalmoplegia (Orphanet:83619)
Mal de Meleda (Orphanet:87503)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Median nodule of the upper lip (Orphanet:2699)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Miller-Dieker syndrome (Orphanet:531)
Mucocutaneous venous malformations (Orphanet:2451)
Neu-Laxova syndrome (Orphanet:2671)
Noonan syndrome (Orphanet:648)
Ondine syndrome (Orphanet:661)
Oral submucous fibrosis (Orphanet:357154)
PAROTID SALIVARY GLANDS, POLYCYSTIC DYSGENETIC DISEASE OF (OMIM:600343)
PEHO syndrome (Orphanet:2836)
Palmoplantar keratoderma-esophageal carcinoma syndrome (Orphanet:2198)
Peutz-Jeghers syndrome (Orphanet:2869)
Piebaldism (Orphanet:2884)
Pyknoachondrogenesis (Orphanet:3003)
SALIVARY DUCT CALCULI (OMIM:181010)
Sarcoidosis (Orphanet:797)
Schwartz-Jampel syndrome (Orphanet:800)
Syngnathia multiple anomalies (Orphanet:3262)
TONGUE CURLING, FOLDING, OR ROLLINGCLOVERLEAF TONGUE, INCLUDED (OMIM:189300)
Transcobalamin deficiency (Orphanet:859)
Treacher-Collins syndrome (Orphanet:861)
Trigonocephaly - broad thumbs (Orphanet:3365)
Tubulointerstitial nephritis and uveitis syndrome (Orphanet:91500)
Waardenburg syndrome (Orphanet:3440)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked intellectual deficit - cerebellar hypoplasia (Orphanet:137831)
[DEL] PSEUDOXANTHOMA ELASTICUM (OMIM:264800)