Abnormality of the hairline
Symptom Information:
All diseases associated with this symptom:
16q24.3 microdeletion syndrome | (Orphanet:261250) |
1p36 deletion syndrome | (Orphanet:1606) |
8q22.1 microdeletion syndrome | (Orphanet:178303) |
Ablepharon macrostomia syndrome | (Orphanet:920) |
Acrofacial dysostosis, Catania type | (Orphanet:1786) |
Beckwith-Wiedemann syndrome due to NSD1 mutation | (Orphanet:238613) |
Braddock syndrome | (Orphanet:52047) |
C syndrome | (Orphanet:1308) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Disorder of sex development - intellectual deficit | (Orphanet:2983) |
Distal trisomy 18q | (Orphanet:1716) |
Facial ectodermal dysplasia | (Orphanet:1807) |
Fraser syndrome | (Orphanet:2052) |
Gonadal dysgenesis, XY type - associated anomalies | (Orphanet:1770) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Intellectual deficit, X-linked - seizures - psoriasis | (Orphanet:3052) |
Intellectual deficit, X-linked, Vitale type | (Orphanet:85289) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
Marden-Walker syndrome | (Orphanet:2461) |
Micrencephaly - corpus callosum agenesis - abnormal genitalia | (Orphanet:2508) |
Oculotrichoanal syndrome | (Orphanet:2717) |
PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER) | (OMIM:614886) |
Pachydermoperiostosis | (Orphanet:2796) |
Prader-Willi syndrome | (Orphanet:739) |
Prominent glabella - microcephaly - hypogenitalism | (Orphanet:2083) |
Ring chromosome 1 | (Orphanet:1437) |
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion | (Orphanet:353281) |
SCARF syndrome | (Orphanet:3134) |
Trisomy 4p | (Orphanet:1738) |