Narrow palate
Symptom Information:
Symptom ID: | HPO:0000189 | ||||||
Synonyms: |
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Quality: | |||||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |