Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C3494506
Disease: Pseudohypoparathyroidism, Type Ia
Pseudohypoparathyroidism, Type Ia 		30 0 22 0.73 0 0
CUI: C0033806
Disease: Pseudohypoparathyroidism
Pseudohypoparathyroidism 		34 0 16 0.40 0 0
CUI: C1864100
Disease: PSEUDOHYPOPARATHYROIDISM, TYPE IB
PSEUDOHYPOPARATHYROIDISM, TYPE IB 		13 0 9 0.35 0 0
CUI: C0033835
Disease: Pseudopseudohypoparathyroidism
Pseudopseudohypoparathyroidism 		14 0 9 0.33 0 0
CUI: C2932715
Disease: Pseudohypoparathyroidism Type 1B
Pseudohypoparathyroidism Type 1B 		8 0 7 0.30 0 0
CUI: C2932716
Disease: Pseudohypoparathyroidism Type 1C
Pseudohypoparathyroidism Type 1C 		4 0 4 0.18 0 0
CUI: C3267007
Disease: Hypercalcitoninaemia
Hypercalcitoninaemia 		7 0 4 0.16 0 0
CUI: C2931817
Disease: Chromosome 2q37 deletion syndrome
Chromosome 2q37 deletion syndrome 		9 0 4 0.15 0 0
CUI: C0857973
Disease: Elevated circulating parathyroid hormone level
Elevated circulating parathyroid hormone level 		18 0 5 0.14 0 0
CUI: C1864105
Disease: Low urinary cyclic AMP response to PTH administration
Low urinary cyclic AMP response to PTH administration 		3 0 3 0.14 0 0
CUI: C2062372
Disease: Adrenal hyperplasia, bilateral
Adrenal hyperplasia, bilateral 		12 0 4 0.13 0 0
CUI: C1300206
Disease: Blomstrand dysplasia
Blomstrand dysplasia 		4 0 3 0.13 0 0
CUI: C2937224
Disease: Constitutional obesity
Constitutional obesity 		6 0 3 0.12 0 0
CUI: C0264009
Disease: Osteodystrophy
Osteodystrophy 		7 0 3 0.12 0 0
CUI: C2940785
Disease: HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3 		8 0 3 0.11 0 0
CUI: C0239803
Disease: Red hair
Red hair 		9 0 3 0.11 0 0
CUI: C1449843
Disease: Pseudohypoaldosteronism, Type I, Autosomal Recessive
Pseudohypoaldosteronism, Type I, Autosomal Recessive 		10 0 3 0.10 0 0
CUI: C2713447
Disease: Hyperpotassemia and Hypertension, Familial
Hyperpotassemia and Hypertension, Familial 		10 0 3 0.10 0 0
CUI: C1449842
Disease: Pseudohypoaldosteronism, Type I, Autosomal Dominant
Pseudohypoaldosteronism, Type I, Autosomal Dominant 		13 0 3 9.4E-02 0 0
CUI: C0278864
Disease: Growth Hormone-Producing Pituitary Gland Neoplasm
Growth Hormone-Producing Pituitary Gland Neoplasm 		14 0 3 9.1E-02 0 0
CUI: C0342346
Disease: Pseudohypoparathyroidism and pseudopseudohypoparathyroidism
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism 		2 0 2 9.1E-02 0 0
CUI: C0745106
Disease: hyperparathyroid
hyperparathyroid 		14 0 3 9.1E-02 0 0
CUI: C1266018
Disease: Hepatocellular carcinoma, scirrhous
Hepatocellular carcinoma, scirrhous 		2 0 2 9.1E-02 0 0
CUI: C1300261
Disease: Acroscyphodysplasia
Acroscyphodysplasia 		2 0 2 9.1E-02 0 0
CUI: C1504412
Disease: Testotoxicosis
Testotoxicosis 		14 0 3 9.1E-02 0 0