Pages that link to "XX gonadal dysgenesis"
From WikiMD's Wellness Encyclopedia
The following pages link to XX gonadal dysgenesis:
Displayed 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Osteopetrosis (← links | edit)
- Donohue syndrome (← links | edit)
- Glanzmann thrombasthenia (← links | edit)
- Laron syndrome (← links | edit)
- Thanatophoric dysplasia (← links | edit)
- Waardenburg syndrome (← links | edit)
- Nevoid basal cell carcinoma syndrome (← links | edit)
- Familial hypercholesterolemia (← links | edit)
- Selective IgA deficiency (← links | edit)
- Miscellaneous (← links | edit)
- Health topics a-z (← links | edit)
- Gonadotropin-releasing hormone insensitivity (← links | edit)
- Antley–Bixler syndrome (← links | edit)
- Cenani–Lenz syndactylism (← links | edit)
- Follicle-stimulating hormone insensitivity (← links | edit)
- Leukocyte adhesion deficiency-1 (← links | edit)
- Loeys–Dietz syndrome (← links | edit)
- TNF receptor associated periodic syndrome (← links | edit)
- WHIM syndrome (← links | edit)
- Worth syndrome (← links | edit)
- Health-encyclopedia-X (← links | edit)
- Gonadal dysgenesis, XX type (redirect page) (← links | edit)
- List of diseases (G) (← links | edit)
- List of rare diseases-G (← links | edit)
- Gonadal dysgenesis, XX type, with deafness (redirect page) (← links | edit)
- List of rare diseases-G (← links | edit)
- Genetic diseases-G (← links | edit)
- Ovarian dysgenesis with sensorineural deafness (redirect page) (← links | edit)
- List of rare diseases-O (← links | edit)
- Genetic diseases-O (← links | edit)
- X-linked severe combined immunodeficiency (← links | edit)
- Kallmann syndrome (← links | edit)
- Hereditary hemorrhagic telangiectasia (← links | edit)
- Familial exudative vitreoretinopathy (← links | edit)
- Common variable immunodeficiency (← links | edit)
- Crouzon syndrome (← links | edit)
- Congenital amegakaryocytic thrombocytopenia (← links | edit)
- Congenital insensitivity to pain with anhidrosis (← links | edit)
- Apert syndrome (← links | edit)
- Template:Cell surface receptor deficiencies (← links | edit)
- Category:Congenital disorders of male genital organs (← links | edit)
- Gastrointestinal Stromal Tumors (← links | edit)
- Tumor necrosis factor receptor-associated periodic syndrome (← links | edit)
- Nephrogenic diabetes insipidus (← links | edit)
- Worth type autosomal dominant osteosclerosis (← links | edit)
- Juvenile polyposis syndrome (← links | edit)
- Category:Congenital disorders of female genital organs (← links | edit)
- Familial hypocalciuric hypercalcemia type 1 (← links | edit)
- Familial hypocalciuric hypercalcemia type 3 (← links | edit)
- Kallmann syndrome 1 (← links | edit)
- Dietz syndrome (← links | edit)
- Pseudohypoparathyroidism type 1A (← links | edit)
- Pseudohypoparathyroidism type 1B (← links | edit)
- Pseudohypoparathyroidism type 2 (← links | edit)
- Leukocyte adhesion deficiency type 1 (← links | edit)
- Achondroplasia (← links | edit)