Non-midline cleft lip
Symptom Information:
Symptom ID: | HPO:0100335 | |||||||||||||||||
Synonyms: |
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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 lip(HPO:0000159) Abnormality of upper lip(HPO:0000177) Cleft upper lip(HPO:0000204) Non-midline cleft lip(HPO:0100335) Oral cleft(HPO:0000202) Cleft upper lip(HPO:0000204) Non-midline cleft lip(HPO:0100335) MedDRA: |
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Database Frequency: | 12 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
Absent tibia - polydactyly - arachnoid cyst | (Orphanet:3328) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
Familial gastric cancer | (Orphanet:26106) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Lymphedema - distichiasis | (Orphanet:33001) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13 | (OMIM:613192) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 | (OMIM:236670) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 | (OMIM:613150) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Oculoauriculovertebral spectrum with radial defects | (Orphanet:2549) |
Steinert myotonic dystrophy | (Orphanet:273) |
TMCO1 defect syndrome | (Orphanet:228407) |