Disease browser and phenotype portal

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MSeqDR-LSDB
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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Hearing Loss Disease Portal

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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes

Disease Browser
Parent Node: Follicular Cyst (D005497)
Parent Node: Neoplasms, Basal Cell (D018295)
Parent Node: Skin Neoplasms (D012878)
..Starting node ..Trichofolliculoma (C536553)
Child Nodes:
Sister Nodes:
..Abdominal chemodectomas with cutaneous angiolipomas (C535552)
..Acanthoma (D049309)
..Bazex-Dupre-Christol syndrome (C537663)
..Becker Nevus Syndrome (C565735)
..Blue rubber bleb nevus syndrome (C536240)
..Calcifying Epithelial Odontogenic Tumor (C537961)
..Cardiomyopathy hypogonadism collagenoma syndrome (C535582)
..Collagenoma, Familial Cutaneous (C562925)
..Davenport Donlan syndrome (C535988)
..Dermatopathia pigmentosa reticularis (C535374)
..Familial cylindromatosis (C536611)
..Familial multiple trichodiscomas (C536847)
..Fanconi like syndrome (C536855)
..Giant pigmented hairy nevus (C536819)
..Hamartoma, Precalcaneal Congenital Fibrolipomatous (C565226)
..Histiocytosis, Progressive Mucinous (C564186)
..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1 (OMIM:155600)
..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 (OMIM:155601)
..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3 (OMIM:609048)
..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 4 (OMIM:608035)
..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5 (OMIM:613099)
..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 7 (OMIM:612263)
..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8 (OMIM:614456)
..Nevus, Epidermal (C562736)
..PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL (OMIM:610644)
..Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal (C565693)
..Papillomatosis, Familial Cutaneous (C566832)
..Phacomatosis pigmentokeratotica (C537893)
..Reactive angioendotheliomatosis (C535293)
..Reed's syndrome (C535516)
..Rombo syndrome (C535870)
..Schwannomatosis (C536641)
..Sclerotylosis (C537526)
..Sebaceous Gland Neoplasms (D012626) 2
..Sweat Gland Neoplasms (D013544)
..Trichoepithelioma, Multiple Familial, 2 (C567418)
..Trichoepitheliomas, Multiple Desmoplastic (C566034)
..Trichofolliculoma (C536553)
..Tufted angioma (C536924)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11234
Name:	Trichofolliculoma
Definition:
Alternative IDs:
ParentIDs:	MESH:D005497\|MESH:D012878\|MESH:D018295
TreeNumbers:	C04.182.300/C536553 \|C04.557.470.565/C536553 \|C04.588.805/C536553 \|C17.800.882/C536553
Synonyms:	Congenital trichofolliculoma \|Recurrent trichofolliculoma \|Sebaceous trichofolliculoma
Slim Mappings:	Cancer\|Skin disease
Reference:	MedGen: C536553 MeSH: C536553 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants