has material basis in germline mutation in SREBF1 hereditary mucoepithelial dysplasia https://rarediseases.info.nih.gov/diseases/5427/hereditary-mucoepithelial-dysplasia https://www.malacards.org/card/mucoepithelial_dysplasia_hereditary Urban-Schosser-Spohn syndrome HMD OMIM:158310 A condition that affects the skin, hair, mucosa (areas ofthe body that are lined with mucus), gums (gingiva), eyes, nose and lungs. Symptoms typically begin in infancy and may include development of cataracts (clouding of the eye lens); blindness; hair loss (alopecia); abnormal changes to the perineum (the area between the anus and external genitalia); and small, skin-colored bumps (keratosis pilaris). Terminal lung disease has also been reported. The cause of HMD is thought to be an abnormality in desmosomes and gap junctions, which are structures involved in cell-to-cell contact. HMD typically follows autosomal dominant inheritance, but has occurred sporadically (in an individual who has no family history of the condition). Treatment typically focuses on individual symptoms of the condition. MESH:C536476 SCTID:403442005 MEDGEN:220887 mucoepithelial dysplasia, hereditary icd11.foundation:1167609602 Orphanet:1839 MONDO:0008017 GARD:0005427 ICD9:478.79 UMLS:C1274795 hereditary skin disorder