Open mouth

Symptom Information:

Symptom ID: HPO:0000194
Synonyms:
OPEN MOUTH APPEARANCE [HPO:0000194]
Mouth held open [Orphanet:9360]
Open mouth [OMIM:Open mouth]
Open mouth appearance [OMIM:Open mouth appearance]
Mouth open [OMIM:Mouth open]
Open mouth (deletion patients) [OMIM:Open mouth (deletion patients)]
Quality:
Cross references:
Orphanet:9360 "Mouth held open" [Orphanet:9360]
OMIM: "Open mouth" [OMIM:Open mouth]
OMIM: "Open mouth appearance" [OMIM:Open mouth appearance]
OMIM: "Mouth open" [OMIM:Mouth open]
OMIM: "Open mouth (deletion patients)" [OMIM:Open mouth (deletion patients)]
Is a (Direct Parents):
Orphanet Abnormality of the mouth
HPO         Abnormality of mouth shape
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 mouth shape(HPO:0011338)
                      Open mouth(HPO:0000194)
MedDRA:
Database Frequency: 70 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
16p11.2p12.2 microdeletion syndrome (Orphanet:261211)
2q23.1 microdeletion syndrome (Orphanet:228402)
5q14.3 microdeletion syndrome (Orphanet:228384)
Aase-Smith syndrome (Orphanet:916)
Acrocallosal syndrome (Orphanet:36)
Acrodysostosis (Orphanet:950)
Adducted thumbs - arthrogryposis, Christian type (Orphanet:2952)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Autosomal dominant nonsyndromic intellectual deficit (Orphanet:178469)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carpenter-Waziri syndrome (Orphanet:93973)
Christianson syndrome (Orphanet:85278)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Coffin-Lowry syndrome (Orphanet:192)
Cohen syndrome (Orphanet:193)
Craniofacial dyssynostosis (Orphanet:1516)
Down syndrome (Orphanet:870)
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY (OMIM:600906)
Fetal Gaucher disease (Orphanet:85212)
German syndrome (Orphanet:2077)
Hereditary sensory and autonomic neuropathy type 6 (Orphanet:314381)
Holmes-Gang syndrome (Orphanet:93970)
Intellectual deficit - hypotonia - skin hyperpigmentation (Orphanet:3050)
Intellectual deficit, X-linked - hypotonia - facial dysmorphism - aggressive behavior (Orphanet:85329)
Intellectual deficit, X-linked - seizures - psoriasis (Orphanet:3052)
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome (Orphanet:369837)
Joubert syndrome 14 (OMIM:614424)
Joubert syndrome with ocular defect (Orphanet:220493)
Juberg-Marsidi syndrome (Orphanet:93972)
KEPPEN-LUBINSKY SYNDROME (OMIM:614098)
Koolen-De Vries syndrome (Orphanet:96169)
LUJAN-FRYNS SYNDROME (OMIM:309520)
Large congenital melanocytic nevus (Orphanet:626)
Lethal restrictive dermopathy (Orphanet:1662)
Lichstenstein syndrome (Orphanet:2390)
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTICFEATURES (OMIM:613670)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 27 (OMIM:615866)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 31 (OMIM:616158)
MENTAL RETARDATION, X-LINKED 21 (OMIM:300143)
MENTAL RETARDATION, X-LINKED 30 (OMIM:300558)
MGAT2-CDG (Orphanet:79329)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 (OMIM:613156)
Marshall-Smith syndrome (Orphanet:561)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Moebius syndrome (Orphanet:570)
Mowat-Wilson syndrome (Orphanet:2152)
Multiple congenital anomalies - hypotonia - seizures syndrome (Orphanet:280633)
Oculocerebrorenal syndrome (Orphanet:534)
Okamoto syndrome (Orphanet:2729)
PEHO syndrome (Orphanet:2836)
PEHO-like syndrome (Orphanet:99807)
Perlman syndrome (Orphanet:2849)
Pfeiffer syndrome (Orphanet:710)
Pitt-Hopkins syndrome (Orphanet:2896)
Proteus syndrome (Orphanet:744)
Qazi-Markouizos syndrome (Orphanet:3010)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
SCHAAF-YANG SYNDROME (OMIM:615547)
SLC35A2-CDG (Orphanet:356961)
Short rib-polydactyly syndrome (Orphanet:1505)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Smith-Magenis syndrome (Orphanet:819)
VELOCARDIOFACIAL SYNDROME (OMIM:192430)
Williams syndrome (Orphanet:904)
X-linked creatine transporter deficiency (Orphanet:52503)
X-linked distal arthrogryposis multiplex congenita (Orphanet:1145)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)