| Disease Browser
|
Parent Node:
 Abnormalities, Multiple (D000015) | Parent Node:
Cleft Palate (D002972) | Parent Node:
Facies (D019066) | Parent Node:
Intellectual Disability (D008607) | Parent Node:
Vitiligo (D014820) | ..Starting node
.. Schrander-Stumpel Theunissen Hulsmans syndrome (C536639)
|
Child Nodes:
|
Sister Nodes: | ..Alopecia universalis onychodystrophy vitiligo (C537056)
| ..AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:607836)
| ..AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2 (OMIM:608391)
| ..AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3 (OMIM:608392)
| ..AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4 (OMIM:609400)
| ..Deafness, Congenital, with Vitiligo and Achalasia (C565642)
| ..Schrander-Stumpel Theunissen Hulsmans syndrome (C536639)
| ..Spastic paraplegia 23 (C536859)
| ..Vitiligo, Progressive, with Mental Retardation and Urethral Duplication (C564739)
| ..VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (OMIM:606579)
| ..VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 (OMIM:193200)
|
Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
|
|
|
| Term ID: | 10042 |
| Name: | Schrander-Stumpel Theunissen Hulsmans syndrome |
| Definition: | |
| Alternative IDs: | |
| ParentIDs: | MESH:D000015|MESH:D002972|MESH:D008607|MESH:D014820|MESH:D019066 |
| TreeNumbers: | C05.500.460.185/C536639 |C05.660.207.540.460.185/C536639 |C07.320.440.185/C536639 |C07.465.525.185/C536639 |C07.650.500.460.185/C536639 |C07.650.525.185/C536639 |C10.597.606.643/C536639 |C16.131.077/C536639 |C16.131.621.207.540.460.185/C536639 |C16.131.850.500.46 |
| Synonyms: | Vitiligo, psychomotor retardation, cleft palate and facial dysmorphism |Vitiligo vulgaris, cleft palate, somatic and psychomotor retardation and facial dysmorphism |
| Slim Mappings: | Congenital abnormality|Mental disorder|Mouth disease|Musculoskeletal disease|Nervous system disease|Pathology (process)|Signs and symptoms|Skin disease |
| Reference: |
MedGen: C536639
MeSH: C536639
OMIM:
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
|
