Conditions Search
Conditions starting from Sf to Sj
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'Sf to Sj' returned 114 records
- SGA
- Shaken baby syndrome
- Shapiro syndrome
- Sharma Kapoor Ramji syndrome
- Sharp syndrome
- Shaver's disease
- Sheehan syndrome
- Shigellosis
- Shin splints
- Shingles
- Shith Filkins syndrome
- Short Arm Syndrome
- Short bowel syndrome
- Short broad great toe macrocranium
- Short chain acyl CoA dehydrogenase deficiency
- Short limb dwarf edema iris coloboma
- Short limb dwarf lethal Colavita Kozlowski type
- Short limb dwarf lethal Mcalister Crane type
- Short limbs abnormal face congenital heart disease
- Short limbs subluxed knees cleft palate
- Short qt syndrome 1
- Short qt syndrome 2
- Short qt syndrome 3
- Short Rib Polydactyly Syndrome
- Short rib-polydactyly syndrome type 1
- Short rib-polydactyly syndrome type 2
- Short rib-polydactyly syndrome type 3
- Short rib-polydactyly syndrome type 4
- Short rib-polydactyly syndrome, Majewski type
- Short rib-polydactyly syndrome, type V
- Short ribs craniosynostosis polysyndactyly
- Short sleeper
- Short Stature
- Short stature abnormal skin pigmentation mental retardation
- Short stature contractures hypotonia
- Short stature cranial hyperostosis hepatomegaly
- Short stature deafness neutrophil dysfunction
- Short stature dysmorphic face pelvic scapula dysplasia
- Short stature hyperkaliemia acidosis
- Short stature mental retardation eye anomalies
- Short stature mental retardation eye defects
- Short stature microcephaly seizures deafness
- Short stature monodactylous ectrodactyly cleft palate
- Short stature prognathism short femoral necks
- Short stature Robin sequence cleft mandible hand anomalies clubfoot
- Short stature syndrome, Brussels type
- Short stature talipes natal teeth
- Short stature webbed neck heart disease
- Short stature wormian bones dextrocardia
- Short stature, cranial hyperostosis, hepatomegaly and diabetes
- Short stature, idiopathic, autosomal
- Short stature, idiopathic, x-linked
- SHORT syndrome
- Short tarsus absence of lower eyelashes
- Shoulder and thorax deformity congenital heart disease
- Shoulder girdle defect mental retardation familial
- Shprintzen omphalocele syndrome
- Shprintzen syndrome
- Shprintzen-Goldberg craniosynostosis syndrome
- Shprintzen-Goldberg syndrome
- Shwachman syndrome
- Shwachman-Diamond syndrome
- Shwartzman phenomenon
- Shy-Drager syndrome
- Sialadenitis
- Sialic acid storage disease, severe infantile type
- Sialidosis
- Sialuria
- Sialuria, French type
- Sick sinus syndrome 1, autosomal recessive
- Sick sinus syndrome 2, autosomal dominant
- Sick sinus syndrome 3, susceptibility to
- Sickle beta thalassemia
- Sickle cell anemia
- Sickle cell disease
- Sickle cell hemoglobin C disease
- Sickle Cell Trait
- Siderius X-linked mental retardation syndrome
- Sideroblastic Anemia
- Sideroblastic anemia acquired
- Sideroblastic anemia and mitochondrial myopathy
- Sideroblastic anemia pyridoxine-refractory autosomal recessive
- Sideroblastic anemia pyridoxine-responsive autosomal recessive
- Sideroblastic anemia X-linked
- Siderosis
- Siegler Brewer Carey syndrome
- Signet ring cell carcinoma
- Silengo Lerone Pelizza syndrome
- Silicosiderosis
- Silicosis
- Sillence syndrome
- Silver-Russell syndrome
- Silvery hair syndrome
- Simian B virus infection
- Simosa cranio facial syndrome
- Simpson-Golabi-Behmel syndrome
- Sine scleroderma
- Singh Chhaparwal Dhanda syndrome
- Single upper central incisor
- Single Ventricle Defects
- Single ventricular heart
- Singleton Merten syndrome
- Sinonasal undifferentiated carcinoma
- Sinus cancer
- Sinus of valsalva aneurysm
- Sirenomelia
- Sitosterolemia
- Situs Ambiguous
- Situs inversus
- Sixth nerve palsy
- Sjogren's Syndrome
- Sjogren's syndrome, juvenile, secondary to autoimmune disease
- Sjogren-Larsson syndrome
- Sjogren-Mikulicz syndrome