Disease Browser
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Parent Node: Cleft Palate (D002972) | Parent Node: Craniofacial Abnormalities (D019465) | Parent Node: Hand Deformities, Congenital (D006228) | Parent Node: Hearing Loss, Mixed Conductive-Sensorineural (D046089) | ..Starting node ..Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly (C566524)
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Sister Nodes: | ..Deafness-Hypogonadism Syndrome (C564435)
| ..Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly (C566524)
| ..Hypospadias, Hypertelorism, Upper Lid Coloboma, and Mixed-Type Hearing Loss (C566373)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 4070 |
Name: | Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D002972|MESH:D006228|MESH:D019465|MESH:D046089 |
TreeNumbers: | C05.390.408/C566524 |C05.500.460.185/C566524 |C05.660.207.540.460.185/C566524 |C05.660.207/C566524 |C05.660.585.988.425/C566524 |C07.320.440.185/C566524 |C07.465.525.185/C566524 |C07.650.500.460.185/C566524 |C07.650.525.185/C566524 |C09.218.458.341.849/C566524 |C1 |
Synonyms: | |
Slim Mappings: | Congenital abnormality|Ear-nose-throat disease|Mouth disease|Musculoskeletal disease|Nervous system disease|Signs and symptoms |
Reference: |
MedGen: C566524
MeSH: C566524
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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