Narrow palate

Symptom Information:

Symptom ID: HPO:0000189
Synonyms:
Narrow palate [OMIM:Narrow palate]
High vaulted/narrow palate [Orphanet:11150]
Narrow palate (46%) [OMIM:Narrow palate (46%)]
Quality:
Cross references:
HPO:0009080 "Narrow, high-arched palate" [Orphanet:11150]
HPO:0000156 "High-arched palate" [Orphanet:11150]
HPO:0002705 "High, narrow palate" [Orphanet:11150]
Orphanet:11150 "High vaulted/narrow palate" [Orphanet:11150]
OMIM: "Narrow palate" [OMIM:Narrow palate]
OMIM: "Narrow palate (46%)" [OMIM:Narrow palate (46%)]
Is a (Direct Parents):
Orphanet Abnormality of the palate
HPO         Abnormality of the palate
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 palate(HPO:0000174)
                         Narrow palate(HPO:0000189)
MedDRA:
Database Frequency: 45 / 7739
Resource:

All diseases associated with this symptom:

Acro-oto-ocular syndrome (Orphanet:2980)
Acro-renal-mandibular syndrome (Orphanet:958)
Apert syndrome (Orphanet:87)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Blepharophimosis-intellectual deficit syndrome, Verloes type (Orphanet:293725)
Bohring-Opitz syndrome (Orphanet:97297)
CARPENTER SYNDROME 2 (OMIM:614976)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Cerebro-oculo-nasal syndrome (Orphanet:66625)
Cleidocranial dysplasia (Orphanet:1452)
Coffin-Lowry syndrome (Orphanet:192)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Developmental delay with autism spectrum disorder and gait instability (Orphanet:329195)
Dysmorphism - conductive hearing loss - heart defect (Orphanet:289553)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Hallermann-Streiff syndrome (Orphanet:2108)
Hennekam syndrome (Orphanet:2136)
Keipert syndrome (Orphanet:2662)
Koolen-De Vries syndrome (Orphanet:96169)
Leprechaunism (Orphanet:508)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 29 (OMIM:616078)
Marfan syndrome type 1 (Orphanet:284963)
Menkes disease (Orphanet:565)
Metaphyseal chondrodysplasia, Kaitila type (Orphanet:166038)
Mitochondrial myopathy and sideroblastic anemia (Orphanet:2598)
Mowat-Wilson syndrome (Orphanet:2152)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Phocomelia, Schinzel type (Orphanet:2879)
Pontocerebellar hypoplasia type 6 (Orphanet:166073)
Pycnodysostosis (Orphanet:763)
Qazi-Markouizos syndrome (Orphanet:3010)
Ramon syndrome (Orphanet:3019)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency (Orphanet:353284)
Saethre-Chotzen syndrome (Orphanet:794)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Sotos syndrome (Orphanet:821)
TRICHORHINOPHALANGEAL SYNDROME, TYPE I (OMIM:190350)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Velo-facial-skeletal syndrome (Orphanet:3424)
WARBURG MICRO SYNDROME 3 (OMIM:614222)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)
Weill-Marchesani syndrome (Orphanet:3449)