Abnormality of the mouth
Symptom Information:
Symptom ID: | HPO:0000153 | |||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | ||||||||||||
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) |
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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) |