| Disease ID | Source | Name | Description |
| 604379 | OMIM | Hypotrichosis 7 (HYPT7) | A condition characterized by the presence of less than the normal amount of hair. Affected individuals have sparse or absent scalp, axillary and body hair and sparse eyebrows and eyelashes. HYPT7 inheritance is autosomal recessive. The disease is caused by variants affecting the gene represented in this entry. |
| 604379 | OMIM | Hypotrichosis 7 (HYPT7) | A condition characterized by the presence of less than the normal amount of hair. Affected individuals have sparse or absent scalp, axillary and body hair and sparse eyebrows and eyelashes. HYPT7 inheritance is autosomal recessive. The disease is caused by variants affecting the gene represented in this entry. |