has material basis in germline mutation in SLC25A24 Fontaine progeroid syndrome https://github.com/monarch-initiative/mondo/issues/1567 https://github.com/monarch-initiative/mondo/issues/9285 https://rarediseases.info.nih.gov/diseases/4497/progeroid-syndrome-petty-type https://www.malacards.org/card/fontaine_progeroid_syndrome Petty Laxova Wiedemann syndrome Fontaine progeroid syndrome MEDGEN:394125 MESH:C537290 craniofacial dysostosis, hypertrichosis, Hypoplasia of labia majora, dental and eye anomalies, patent ductus arteriosus, and normal intelligence craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies OMIM:612289 UMLS:C2676780 Orphanet:697101 Gorlin-Chaudhry-Moss syndrome dental and eye anomalies, patent ductus arteriosus, and normal intelligence progeroid syndrome, Petty type dental and eye anomalies-patent ductus arteriosus-normal intelligence syndrome craniofacial dysostosis, hypertrichosis, hypoplasia of labia majora GCM syndrome NORD:1201 progeroid syndrome congenital Petty type Gorlin Chaudhry Moss syndrome progeroid syndrome, congenital, Petty type A rare premature aging syndrome characterized by pre-and postnatal growth retardation, a congenital premature-aged appearance with distinctive craniofacial dysmorphism (wide calvaria with large open anterior fontanel and wide metopic suture, broad forehead, small face, micrognathia), markedly diminished subcutaneous fat, cutis laxa and wrinkled skin, without delay in psychomotor development. Scant, brittle hair, hypoplastic nails and delayed, abnormal dentition, as well as hypoplastic distal phalanges, umbilical hernia and eye abnormalities (myopia/hyperopia, strabismus), are also commonly associated. GCMS Orphanet:2963 progeroid syndrome Petty type OMIM:233500 cranofacial dysostosis-hypertrichosis-hypoplasia of labia majora syndrome DOID:0051067 GARD:0004497 Orphanet:2095 craniofacial dysostosis-genital, dental, cardiac anomalies syndrome ICD9:759.89 Petty syndrome FPS Gorlin-Chaudhry-Moss Syndrome Petty-Laxova-Wiedemann syndrome MONDO:0012853 SCTID:205800003 multiple congenital anomalies/dysmorphic syndrome without intellectual disability progeroid syndrome ectodermal dysplasia syndrome