Submucous cleft hard palate
Symptom Information:
Symptom ID: | HPO:0000176 | |||||||||||||||||||
Synonyms: |
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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) Abnormality of the hard palate(HPO:0100737) Cleft palate(HPO:0000175) Submucous cleft hard palate(HPO:0000176) Oral cleft(HPO:0000202) Cleft palate(HPO:0000175) Submucous cleft hard palate(HPO:0000176) MedDRA: |
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Database Frequency: | 19 / 7739 | |||||||||||||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
48,XXYY syndrome | (Orphanet:10) |
Bencze syndrome | (Orphanet:1241) |
Branchiogenic deafness syndrome | (Orphanet:50815) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Dubowitz syndrome | (Orphanet:235) |
Gordon syndrome | (Orphanet:376) |
HOLOPROSENCEPHALY 2 | (OMIM:157170) |
Hyaluronidase deficiency | (Orphanet:67041) |
Lethal restrictive dermopathy | (Orphanet:1662) |
MEIER-GORLIN SYNDROME 5 | (OMIM:613805) |
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus | (Orphanet:83473) |
Mowat-Wilson syndrome | (Orphanet:2152) |
OROFACIAL CLEFT 6, SUSCEPTIBILITY TO | (OMIM:608864) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Schilbach-Rott syndrome | (Orphanet:2353) |
Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence | (Orphanet:3201) |
W syndrome | (Orphanet:2804) |